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rs137853320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853320(C;T)
Make rs137853320(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50916059
GeneBMP15
is asnp
is mentioned by
dbSNPrs137853320
ebirs137853320
HLIrs137853320
Exacrs137853320
Varsomers137853320
Maprs137853320
PheGenIrs137853320
hapmaprs137853320
1000 genomesrs137853320
hgdprs137853320
ensemblrs137853320
gopubmedrs137853320
geneviewrs137853320
scholarrs137853320
googlers137853320
pharmgkbrs137853320
gwascentralrs137853320
openSNPrs137853320
23andMers137853320
23andMe allrs137853320
SNP Nexus

SNPshotrs137853320
SNPdbers137853320
MSV3drs137853320
GWAS Ctlgrs137853320
Max Magnitude0
OMIM300247
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853320(T;T)
Alt rs137853320(T;T)
Reference rs137853320(C;C)
Significance Pathogenic
Disease Premature ovarian failure 4
Variation info
Gene BMP15
CLNDBN Premature ovarian failure 4
Reversed 0
HGVS NC_000023.10:g.50659059C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012228.20,