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rs11170547

From SNPedia

Orientationplus
Stabilizedplus
Make rs11170547(C;C)
Make rs11170547(C;T)
Make rs11170547(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position53419219
is asnp
is mentioned by
dbSNPrs11170547
ebirs11170547
HLIrs11170547
Exacrs11170547
Varsomers11170547
Maprs11170547
PheGenIrs11170547
hapmaprs11170547
1000 genomesrs11170547
hgdprs11170547
ensemblrs11170547
gopubmedrs11170547
geneviewrs11170547
scholarrs11170547
googlers11170547
pharmgkbrs11170547
gwascentralrs11170547
openSNPrs11170547
23andMers11170547
23andMe allrs11170547
SNP Nexus

SNPshotrs11170547
SNPdbers11170547
MSV3drs11170547
GWAS Ctlgrs11170547
GMAF0.04224
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23544102OA-icon.png] Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause


[PMID 21193543] Genes involved in initial follicle recruitment may be associated with age at menopause.