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rs104894765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894765(A;G)
Make rs104894765(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50916132
GeneBMP15
is asnp
is mentioned by
dbSNPrs104894765
ebirs104894765
HLIrs104894765
Exacrs104894765
Varsomers104894765
Maprs104894765
PheGenIrs104894765
hapmaprs104894765
1000 genomesrs104894765
hgdprs104894765
ensemblrs104894765
gopubmedrs104894765
geneviewrs104894765
scholarrs104894765
googlers104894765
pharmgkbrs104894765
gwascentralrs104894765
openSNPrs104894765
23andMers104894765
23andMe allrs104894765
SNP Nexus

SNPshotrs104894765
SNPdbers104894765
MSV3drs104894765
GWAS Ctlgrs104894765
Max Magnitude0
OMIM300247
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894765(G;G)
Alt rs104894765(G;G)
Reference rs104894765(A;A)
Significance Pathogenic
Disease Ovarian dysgenesis 2
Variation info
Gene BMP15
CLNDBN Ovarian dysgenesis 2
Reversed 0
HGVS NC_000023.10:g.50659132A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012225.20,