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rs587777872

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777872(C;T)
Make rs587777872(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position118924038
GeneMCM9
is asnp
is mentioned by
dbSNPrs587777872
ebirs587777872
HLIrs587777872
Exacrs587777872
Varsomers587777872
Maprs587777872
PheGenIrs587777872
hapmaprs587777872
1000 genomesrs587777872
hgdprs587777872
ensemblrs587777872
gopubmedrs587777872
geneviewrs587777872
scholarrs587777872
googlers587777872
pharmgkbrs587777872
gwascentralrs587777872
openSNPrs587777872
23andMers587777872
23andMe allrs587777872
SNP Nexus

SNPshotrs587777872
SNPdbers587777872
MSV3drs587777872
GWAS Ctlgrs587777872
Max Magnitude0
ClinVar
Risk rs587777872(T;T)
Alt rs587777872(T;T)
Reference rs587777872(C;C)
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.119245203G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144732.1, RCV000149816.3,