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rs17431357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs17431357(C;T)
Make rs17431357(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120442631
GeneTRIAP1
is asnp
is mentioned by
dbSNPrs17431357
dbSNP (classic)rs17431357
ClinGenrs17431357
ebirs17431357
HLIrs17431357
Exacrs17431357
Gnomadrs17431357
Varsomers17431357
LitVarrs17431357
Maprs17431357
PheGenIrs17431357
Biobankrs17431357
1000 genomesrs17431357
hgdprs17431357
ensemblrs17431357
geneviewrs17431357
scholarrs17431357
googlers17431357
pharmgkbrs17431357
gwascentralrs17431357
openSNPrs17431357
23andMers17431357
SNPshotrs17431357
SNPdbers17431357
MSV3drs17431357
GWAS Ctlgrs17431357
GMAF0.02984
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21901158OA-icon.png]
Trait
Title Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
Risk Allele C
P-val 0.000001
Odds Ratio 34.0000 [22.00 - 44.00] % decrease