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rs10501320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10501320(C;C)
Make rs10501320(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47272248
GeneMADD
is asnp
is mentioned by
dbSNPrs10501320
ebirs10501320
HLIrs10501320
Exacrs10501320
Varsomers10501320
Maprs10501320
PheGenIrs10501320
hapmaprs10501320
1000 genomesrs10501320
hgdprs10501320
ensemblrs10501320
gopubmedrs10501320
geneviewrs10501320
scholarrs10501320
googlers10501320
pharmgkbrs10501320
gwascentralrs10501320
openSNPrs10501320
23andMers10501320
23andMe allrs10501320
SNP Nexus

SNPshotrs10501320
SNPdbers10501320
MSV3drs10501320
GWAS Ctlgrs10501320
GMAF0.1212
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21873549OA-icon.png]
Trait
Title Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Risk Allele G
P-val 1E-88
Odds Ratio None None

[PMID 17357082OA-icon.png] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.