Have questions? Visit https://www.reddit.com/r/SNPedia

rs2059806

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2059806(A;A)
Make rs2059806(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position7166365
GeneINSR
is asnp
is mentioned by
dbSNPrs2059806
ebirs2059806
HLIrs2059806
Exacrs2059806
Varsomers2059806
Maprs2059806
PheGenIrs2059806
hapmaprs2059806
1000 genomesrs2059806
hgdprs2059806
ensemblrs2059806
gopubmedrs2059806
geneviewrs2059806
scholarrs2059806
googlers2059806
pharmgkbrs2059806
gwascentralrs2059806
openSNPrs2059806
23andMers2059806
23andMe allrs2059806
SNP Nexus

SNPshotrs2059806
SNPdbers2059806
MSV3drs2059806
GWAS Ctlgrs2059806
GMAF0.2342
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 21637951] A common variant in the adiponectin gene and polycystic ovary syndrome risk

[PMID 18603647OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.


[PMID 25927028OA-icon.png] An Association Study between INSR/NsiI (rs2059806) and INSR/PmlI (rs1799817) SNPs in Women with Polycystic Ovary Syndrome from West Azerbaijan Province, Iran


ClinVar
Risk rs2059806(A;A)
Alt rs2059806(A;A)
Reference rs2059806(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene INSR
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.7166376C>T
CLNSRC
CLNACC RCV000180111.1,