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rs587777270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCC;CCC) 0 common in clinvar
(GG;GG) 0 common in clinvar
Make rs587777270(C;C)
Make rs587777270(C;GG)
ReferenceGRCh38 38.1/142
Chromosome1
Position91266061
GeneHFM1
is asnp
is mentioned by
dbSNPrs587777270
ebirs587777270
HLIrs587777270
Exacrs587777270
Varsomers587777270
Maprs587777270
PheGenIrs587777270
hapmaprs587777270
1000 genomesrs587777270
hgdprs587777270
ensemblrs587777270
gopubmedrs587777270
geneviewrs587777270
scholarrs587777270
googlers587777270
pharmgkbrs587777270
gwascentralrs587777270
openSNPrs587777270
23andMers587777270
23andMe allrs587777270
SNP Nexus

SNPshotrs587777270
SNPdbers587777270
MSV3drs587777270
GWAS Ctlgrs587777270
Max Magnitude0
ClinVar
Risk rs587777270(CC,GGC;CC,GGC)
Alt rs587777270(CC,GGC;CC,GGC)
Reference rs587777270(CCC;CCC)
Significance Pathogenic
Disease Premature ovarian failure 9
Variation info
Gene HFM1
CLNDBN Premature ovarian failure 9
Reversed 1
HGVS NC_000001.10:g.91731618_91731619delGGinsC
CLNSRC OMIM Allelic Variant
CLNACC RCV000114371.3,