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rs2059807

From SNPedia

Orientationminus
Stabilizedplus
Make rs2059807(C;C)
Make rs2059807(C;T)
Make rs2059807(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position7166098
GeneINSR
is asnp
is mentioned by
dbSNPrs2059807
ebirs2059807
HLIrs2059807
Exacrs2059807
Varsomers2059807
Maprs2059807
PheGenIrs2059807
hapmaprs2059807
1000 genomesrs2059807
hgdprs2059807
ensemblrs2059807
gopubmedrs2059807
geneviewrs2059807
scholarrs2059807
googlers2059807
pharmgkbrs2059807
gwascentralrs2059807
openSNPrs2059807
23andMers2059807
23andMe allrs2059807
SNP Nexus

SNPshotrs2059807
SNPdbers2059807
MSV3drs2059807
GWAS Ctlgrs2059807
GMAF0.449
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21645371OA-icon.png] Family association study between INSR gene polymorphisms and PCOS in Han Chinese

[PMID 18194558OA-icon.png] A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

GWAS snp
PMID [PMID 22885925]
Trait Polycystic ovary syndrome
Title Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.
Risk Allele G
P-val 1E-8
Odds Ratio 1.14 [NR]