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rs16962638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16962638(A;G)
Make rs16962638(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position103534569
is asnp
is mentioned by
dbSNPrs16962638
ebirs16962638
HLIrs16962638
Exacrs16962638
Varsomers16962638
Maprs16962638
PheGenIrs16962638
hapmaprs16962638
1000 genomesrs16962638
hgdprs16962638
ensemblrs16962638
gopubmedrs16962638
geneviewrs16962638
scholarrs16962638
googlers16962638
pharmgkbrs16962638
gwascentralrs16962638
openSNPrs16962638
23andMers16962638
23andMe allrs16962638
SNP Nexus

SNPshotrs16962638
SNPdbers16962638
MSV3drs16962638
GWAS Ctlgrs16962638
GMAF0.02755
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio 15.0000 [8.00 - 22.00] % increase