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rs12655917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12655917(A;A)
Make rs12655917(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position77996116
is asnp
is mentioned by
dbSNPrs12655917
ebirs12655917
HLIrs12655917
Exacrs12655917
Varsomers12655917
Maprs12655917
PheGenIrs12655917
hapmaprs12655917
1000 genomesrs12655917
hgdprs12655917
ensemblrs12655917
gopubmedrs12655917
geneviewrs12655917
scholarrs12655917
googlers12655917
pharmgkbrs12655917
gwascentralrs12655917
openSNPrs12655917
23andMers12655917
23andMe allrs12655917
SNP Nexus

SNPshotrs12655917
SNPdbers12655917
MSV3drs12655917
GWAS Ctlgrs12655917
GMAF0.08219
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 6E-7
Odds Ratio 40.0000 [27 - 51] % decrease