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rs6576507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6576507(C;C)
Make rs6576507(C;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position26043247
GeneEPB41L1
is asnp
is mentioned by
dbSNPrs6576507
ebirs6576507
HLIrs6576507
Exacrs6576507
Varsomers6576507
Maprs6576507
PheGenIrs6576507
hapmaprs6576507
1000 genomesrs6576507
hgdprs6576507
ensemblrs6576507
gopubmedrs6576507
geneviewrs6576507
scholarrs6576507
googlers6576507
pharmgkbrs6576507
gwascentralrs6576507
openSNPrs6576507
23andMers6576507
23andMe allrs6576507
SNP Nexus

SNPshotrs6576507
SNPdbers6576507
MSV3drs6576507
GWAS Ctlgrs6576507
GMAF0.03994
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 A
P-val 4E-7
Odds Ratio 14.0000 [8.00-20.00] % increase