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rs12460989

From SNPedia

Orientationplus
Stabilizedplus
Make rs12460989(G;G)
Make rs12460989(G;T)
Make rs12460989(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position4785155
is asnp
is mentioned by
dbSNPrs12460989
ebirs12460989
HLIrs12460989
Exacrs12460989
Varsomers12460989
Maprs12460989
PheGenIrs12460989
hapmaprs12460989
1000 genomesrs12460989
hgdprs12460989
ensemblrs12460989
gopubmedrs12460989
geneviewrs12460989
scholarrs12460989
googlers12460989
pharmgkbrs12460989
gwascentralrs12460989
openSNPrs12460989
23andMers12460989
23andMe allrs12460989
SNP Nexus

SNPshotrs12460989
SNPdbers12460989
MSV3drs12460989
GWAS Ctlgrs12460989
GMAF0.1079
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 22678803] [Polymorphisms of FEM1A gene in patients with polycystic ovary syndrome] [PMID 18757445OA-icon.png] FEM1A and FEM1B: novel candidate genes for polycystic ovary syndrome.