Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777269(C;T)
Make rs587777269(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position91350738
GeneHFM1
is asnp
is mentioned by
dbSNPrs587777269
ebirs587777269
HLIrs587777269
Exacrs587777269
Varsomers587777269
Maprs587777269
PheGenIrs587777269
hapmaprs587777269
1000 genomesrs587777269
hgdprs587777269
ensemblrs587777269
gopubmedrs587777269
geneviewrs587777269
scholarrs587777269
googlers587777269
pharmgkbrs587777269
gwascentralrs587777269
openSNPrs587777269
23andMers587777269
23andMe allrs587777269
SNP Nexus

SNPshotrs587777269
SNPdbers587777269
MSV3drs587777269
GWAS Ctlgrs587777269
Max Magnitude0
ClinVar
Risk rs587777269(C,T;C,T)
Alt rs587777269(C,T;C,T)
Reference rs587777269(G;G)
Significance Pathogenic
Disease Premature ovarian failure 9
Variation info
Gene HFM1
CLNDBN Premature ovarian failure 9
Reversed 1
HGVS NC_000001.10:g.91816295C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114370.2,