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rs587777268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777268(A;C)
Make rs587777268(C;C)
ReferenceGRCh38 38.1/142
Chromosome1
Position91319322
GeneHFM1
is asnp
is mentioned by
dbSNPrs587777268
ebirs587777268
HLIrs587777268
Exacrs587777268
Varsomers587777268
Maprs587777268
PheGenIrs587777268
hapmaprs587777268
1000 genomesrs587777268
hgdprs587777268
ensemblrs587777268
gopubmedrs587777268
geneviewrs587777268
scholarrs587777268
googlers587777268
pharmgkbrs587777268
gwascentralrs587777268
openSNPrs587777268
23andMers587777268
23andMe allrs587777268
SNP Nexus

SNPshotrs587777268
SNPdbers587777268
MSV3drs587777268
GWAS Ctlgrs587777268
Max Magnitude0
ClinVar
Risk rs587777268(C;C)
Alt rs587777268(C;C)
Reference rs587777268(A;A)
Significance Pathogenic
Disease Premature ovarian failure 9
Variation info
Gene HFM1
CLNDBN Premature ovarian failure 9
Reversed 0
HGVS NC_000001.10:g.91784879A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000114369.3,