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SuicideFuel Low IQ is a fate worse than death

armis

armis

Captain
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Jul 3, 2018
Posts
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Poverty + low IQ is a death sentence for low value males.

With a high IQ you can at least cope and feel superior to normies or go into STEM and moneymaxx. With a low IQ, you're fucked.

Only low IQ men can be truecels because we are inferior in every facet of life.
 
OccsX

All of the low IQ jobs are being replaced by AI + robotics.
Soon you will need a high IQ just not to be homeless.
 
over for literally all niggers, there is not 1 singular nigger with an iq higher than 1
 
Ugly+ sickly + weak + low IQ = the worst combination of traits one can have.
 
My IQ is so low I can't cope
 
i am currycel 2/10, low iq, dont know how to socialize, completely over for me, suicidefuel
 
if you're low iq enough you won't realize you're trucel. Ignorance is bliss
 
Poverty + low IQ is a death sentence for low value males.

With a high IQ you can at least cope and feel superior to normies or go into STEM and moneymaxx. With a low IQ, you're fucked.

Only low IQ men can be truecels because we are inferior in every facet of life.
High iq people owe reparations to low iq people
 
Soon you will need a high IQ just not to be homeless.
No. You can become a fighter of freedom in Daesh and similar organizations once the extremist worldwide resurgence kicks in, in milsim videogame.
 
i do think that you need just enough IQ to ascend though. other than that, looks are way more important imo
 
I own an iq lower than average
 
0089-025.png


...

The observed effect sizes of the three replicated individual SNPs are small [see (5) for discussion]. For EduYears, the strongest effect identified (rs9320913) explains 0.022% of phenotypic variance in the replication sample. This R2 corresponds to a difference of ~1 months of schooling per allele. For college completion, the SNP with the strongest estimated effect (rs11584700) has an odds ratio of 0.912 in the replication sample, equivalent to a 1.8 percentage-point difference per allele in the frequency of completing college.

We subsequently conducted a “combined stage” meta-analysis, including both the discovery and replication samples. This analysis revealed additional genome-wide significant SNPs: four for EduYears and three for College. Three of these newly genome-wide significant SNPs (rs1487441, rs11584700, rs4851264) are in linkage disequilibrium with the replicated SNPs. The remaining four are located in different loci and warrant replication attempts in future research: rs7309, a 3′UTR variant in TANK; rs11687170, close to GBX2; rs1056667, a 3′UTR variant in BTN1A1; and rs13401104 in ASB18.

Using the results of the combined meta-analyses of discovery and replication cohorts, we conducted a series of complementary and exploratory supplemental analyses to aid in interpreting and contextualizing the results: gene-based association tests; eQTL analyses of brain and blood tissue data; pathway analysis; functional annotation searches; enrichment analysis for cell-type-specific overlap with H3K4me3 chromatin marks; and predictions of likely gene function using gene-expression data. Table S20 summarizes promising candidate loci identified through follow-up analyses (5). Two regions in particular showed convergent evidence from functional annotation, blood cis-eQTL analyses, and gene-based tests: chromosome 1q32 (including LRRN2, MDM4, and PIK3C2B) and chromosome 6 near the Major Histocompatibility Complex (MHC). We also find evidence that in anterior caudate cells, there is enrichment of H3K4me3 chromatin marks (believed to be more common in active regulatory regions) in the genomic regions implicated by our analyses (fig. S20). Many of the implicated genes have previously been associated with health, central nervous system, or cognitive-process phenotypes in either human-GWAS or model-animal studies (table S22). Gene co-expression analysis revealed that several implicated genes (including BSN, GBX2, LRRN2, and PIK3C2B) are likely involved in pathways related to cognitive processes (such as learning and long-term memory) and neuronal development or function (table S21).

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Using the results of the combined meta-analyses of discovery and replication cohorts, we conducted a series of complementary and exploratory supplemental analyses to aid in interpreting and contextualizing the results: gene-based association tests; eQTL analyses of brain and blood tissue data; pathway analysis; functional annotation searches; enrichment analysis for cell-type-specific overlap with H3K4me3 chromatin marks; and predictions of likely gene function using gene-expression data. Table S20 summarizes promising candidate loci identified through follow-up analyses (5). Two regions in particular showed convergent evidence from functional annotation, blood cis-eQTL analyses, and gene-based tests: chromosome 1q32 (including LRRN2, MDM4, and PIK3C2B) and chromosome 6 near the Major Histocompatibility Complex (MHC). We also find evidence that in anterior caudate cells, there is enrichment of H3K4me3 chromatin marks (believed to be more common in active regulatory regions) in the genomic regions implicated by our analyses (fig. S20). Many of the implicated genes have previously been associated with health, central nervous system, or cognitive-process phenotypes in either human-GWAS or model-animal studies (table S22). Gene co-expression analysis revealed that several implicated genes (including BSN, GBX2, LRRN2, and PIK3C2B) are likely involved in pathways related to cognitive processes (such as learning and long-term memory) and neuronal development or function (table S21).
 
103-png.735713


...

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ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Search:

PopulationGroupSample SizeRef AlleleAlt Allele


PopulationGroupSample SizeRef AlleleAlt Allele
TotalGlobal75648T=0.72342C=0.27658, G=0.00000
EuropeanSub61372T=0.71551C=0.28449, G=0.00000
AfricanSub6260T=0.6947C=0.3053, G=0.0000
African OthersSub204T=0.662C=0.338, G=0.000
African AmericanSub6056T=0.6958C=0.3042, G=0.0000
AsianSub218T=0.908C=0.092, G=0.000
East AsianSub178T=0.899C=0.101, G=0.000
 
0089-039.png


0089-040.png


...

3


1

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ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Search:

PopulationGroupSample SizeRef AlleleAlt Allele


PopulationGroupSample SizeRef AlleleAlt Allele
TotalGlobal159708G=0.804506T=0.195494
EuropeanSub138852G=0.807003T=0.192997
AfricanSub6680G=0.8226T=0.1774
African OthersSub242G=0.826T=0.174
African AmericanSub6438G=0.8225T=0.1775
AsianSub636G=0.436T=0.564
East AsianSub504G=0.415T=0.585
Other AsianSub132G=0.515T=0.485
Latin American 1Sub758G=0.811T=0.189
Latin American 2Sub6320G=0.7983T=0.2017

...

0089-041.png


0089-042.png
 
i would trade IQ points for height
 
IQ helps you moneymaxx so you can afford nice copes (escorts, delicious food and drinks, drugs, gaming and other entertainment etc).
 
Poverty + low IQ is a death sentence for low value males.

With a high IQ you can at least cope and feel superior to normies or go into STEM and moneymaxx. With a low IQ, you're fucked.

Only low IQ men can be truecels because we are inferior in every facet of life.
I think being low IQ in the 3rd world is fine. Even ugly low tier normies working in sweatshops get a looksmatch and have 10 kids.
 
This guy ^ is super right
 
Imagine for a moment that humans did not have eyes, and thus the sense of vision was a completely alien and unimaginable concept to us. Imagine the geniuses among these humans somehow (in their wisdom) deduced the presence and functions of the electromagnetic spectrum across all wavelengths. Imagine them then trying to explain the physics of waves and light to the other (naturally blind) humans.

That is what it's like to be high IQ in a world where the majority are average. Your understanding - and therefore experience - of the world is vastly different. Now imagine how limited the experiences of the world are from the perspective of a low IQ individual. It's downright tragic.

Yes, living as a retard is an existence worse than death, but only from the perspective of someone on the polar opposite side of that. Stupid AND ugly? Holy fuck, it never began.
 

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