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rs17003221

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17003221(C;T)
Make rs17003221(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50916280
GeneBMP15
is asnp
is mentioned by
dbSNPrs17003221
dbSNP (classic)rs17003221
ClinGenrs17003221
ebirs17003221
HLIrs17003221
Exacrs17003221
Gnomadrs17003221
Varsomers17003221
LitVarrs17003221
Maprs17003221
PheGenIrs17003221
Biobankrs17003221
1000 genomesrs17003221
hgdprs17003221
ensemblrs17003221
geneviewrs17003221
scholarrs17003221
googlers17003221
pharmgkbrs17003221
gwascentralrs17003221
openSNPrs17003221
23andMers17003221
SNPshotrs17003221
SNPdbers17003221
MSV3drs17003221
GWAS Ctlgrs17003221
GMAF0.1378
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM300247
DescBONE MORPHOGENETIC PROTEIN 15; BMP15
Variant
Relatedalso


[PMID 18614612OA-icon.png] Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.


ClinVar
Risk rs17003221(T;T)
Alt rs17003221(T;T)
Reference Rs17003221(C;C)
Significance Non-pathogenic
Disease not specified Ovarian Dysgenesis
Variation info
Gene BMP15
CLNDBN not specified Ovarian Dysgenesis
Reversed 0
HGVS NC_000023.10:g.50659280C>T
CLNSRC
CLNACC RCV000245391.2, RCV000292718.1,