Rs104894763

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894763(C;T)
Make rs104894763(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50910985
GeneBMP15
is asnp
is mentioned by
dbSNPrs104894763
PheGenIrs104894763
nextbiors104894763
hapmaprs104894763
1000 genomesrs104894763
hgdprs104894763
ensemblrs104894763
gopubmedrs104894763
geneviewrs104894763
scholarrs104894763
googlers104894763
pharmgkbrs104894763
gwascentralrs104894763
openSNPrs104894763
23andMers104894763
23andMe allrs104894763
SNP Nexus

SNPshotrs104894763
SNPdbers104894763
MSV3drs104894763
GMAF0.0006046
Max Magnitude0
OMIM300247
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894763(T;T)
Alt rs104894763(T;T)
Reference rs104894763(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.50653985C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012229.1,