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

rs587777871

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777871(C;C)
Make rs587777871(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position118827925
GeneMCM9
is asnp
is mentioned by
dbSNPrs587777871
ebirs587777871
HLIrs587777871
Exacrs587777871
Varsomers587777871
Maprs587777871
PheGenIrs587777871
hapmaprs587777871
1000 genomesrs587777871
hgdprs587777871
ensemblrs587777871
gopubmedrs587777871
geneviewrs587777871
scholarrs587777871
googlers587777871
pharmgkbrs587777871
gwascentralrs587777871
openSNPrs587777871
23andMers587777871
23andMe allrs587777871
SNP Nexus

SNPshotrs587777871
SNPdbers587777871
MSV3drs587777871
GWAS Ctlgrs587777871
Max Magnitude0
ClinVar
Risk rs587777871(C;C)
Alt rs587777871(C;C)
Reference rs587777871(T;T)
Significance Pathogenic
Disease Premature ovarian failure 1 Ovarian dysgenesis 4
Variation info
Gene MCM9
CLNDBN Premature ovarian failure 1 Ovarian dysgenesis 4
Reversed 1
HGVS NC_000006.11:g.119149088A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144731.1, RCV000149815.3,