Rs104894766

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894766(C;T)
Make rs104894766(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50911009
GeneBMP15
is asnp
is mentioned by
dbSNPrs104894766
Exacrs104894766
PheGenIrs104894766
nextbiors104894766
hapmaprs104894766
1000 genomesrs104894766
hgdprs104894766
ensemblrs104894766
gopubmedrs104894766
geneviewrs104894766
scholarrs104894766
googlers104894766
pharmgkbrs104894766
gwascentralrs104894766
openSNPrs104894766
23andMers104894766
23andMe allrs104894766
SNP Nexus

SNPshotrs104894766
SNPdbers104894766
MSV3drs104894766
Max Magnitude0
OMIM300247
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894766(T;T)
Alt rs104894766(T;T)
Reference rs104894766(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.50654009C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012226.23,