rs2059807

Orientation

minus

Stabilized

minus

Make rs2059807(C;C)

Make rs2059807(C;T)

Make rs2059807(T;T)

Reference

GRCh38 38.1/142

Chromosome

19

Position

7166098

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs2059807
dbSNP (classic)	rs2059807
ClinGen	rs2059807
ebi	rs2059807
HLI	rs2059807
Exac	rs2059807
Gnomad	rs2059807
Varsome	rs2059807
LitVar	rs2059807
Map	rs2059807
PheGenI	rs2059807
Biobank	rs2059807
1000 genomes	rs2059807
hgdp	rs2059807
ensembl	rs2059807
geneview	rs2059807
scholar	rs2059807
google	rs2059807
pharmgkb	rs2059807
gwascentral	rs2059807
openSNP	rs2059807
23andMe	rs2059807
SNPshot	rs2059807
SNPdbe	rs2059807
MSV3d	rs2059807
GWAS Ctlg	rs2059807

GMAF

0.449

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 21645371 ] Family association study between INSR gene polymorphisms and PCOS in Han Chinese

[PMID 18194558 ] 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]