Rs104894767

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894767(A;A)
Make rs104894767(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50915966
GeneBMP15
is asnp
is mentioned by
dbSNPrs104894767
Exacrs104894767
PheGenIrs104894767
nextbiors104894767
hapmaprs104894767
1000 genomesrs104894767
hgdprs104894767
ensemblrs104894767
gopubmedrs104894767
geneviewrs104894767
scholarrs104894767
googlers104894767
pharmgkbrs104894767
gwascentralrs104894767
openSNPrs104894767
23andMers104894767
23andMe allrs104894767
SNP Nexus

SNPshotrs104894767
SNPdbers104894767
MSV3drs104894767
GMAF0.001209
OMIM300247
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894767(A;A)
Alt rs104894767(A;A)
Reference rs104894767(G;G)
Significance Pathogenic
Disease Premature ovarian failure 4
Variation info
Gene BMP15
CLNDBN Premature ovarian failure 4
Reversed 0
HGVS NC_000023.10:g.50658966G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012227.1,