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rs606231343

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231343(C;G)
Make rs606231343(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position5955211
GeneMCM8
is asnp
is mentioned by
dbSNPrs606231343
ebirs606231343
HLIrs606231343
Exacrs606231343
Varsomers606231343
Maprs606231343
PheGenIrs606231343
hapmaprs606231343
1000 genomesrs606231343
hgdprs606231343
ensemblrs606231343
gopubmedrs606231343
geneviewrs606231343
scholarrs606231343
googlers606231343
pharmgkbrs606231343
gwascentralrs606231343
openSNPrs606231343
23andMers606231343
23andMe allrs606231343
SNP Nexus

SNPshotrs606231343
SNPdbers606231343
MSV3drs606231343
GWAS Ctlgrs606231343
Max Magnitude0
ClinVar
Risk rs606231343(G;G)
Alt rs606231343(G;G)
Reference rs606231343(C;C)
Significance Pathogenic
Disease not provided Premature ovarian failure 10
Variation info
Gene MCM8
CLNDBN not provided Premature ovarian failure 10
Reversed 0
HGVS NC_000020.10:g.5935857C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000148343.1, RCV000162356.4,