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rs6022786

From SNPedia

Orientationplus
Stabilizedplus
Make rs6022786(A;A)
Make rs6022786(A;G)
Make rs6022786(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position53830764
is asnp
is mentioned by
dbSNPrs6022786
ebirs6022786
HLIrs6022786
Exacrs6022786
Varsomers6022786
Maprs6022786
PheGenIrs6022786
hapmaprs6022786
1000 genomesrs6022786
hgdprs6022786
ensemblrs6022786
gopubmedrs6022786
geneviewrs6022786
scholarrs6022786
googlers6022786
pharmgkbrs6022786
gwascentralrs6022786
openSNPrs6022786
23andMers6022786
23andMe allrs6022786
SNP Nexus

SNPshotrs6022786
SNPdbers6022786
MSV3drs6022786
GWAS Ctlgrs6022786
GMAF0.4371
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 A
P-val 2E-9
Odds Ratio 1.13 [NR]