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rs138761187

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138761187(A;A)
Make rs138761187(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position5985921
GeneMCM8
is asnp
is mentioned by
dbSNPrs138761187
ebirs138761187
HLIrs138761187
Exacrs138761187
Varsomers138761187
Maprs138761187
PheGenIrs138761187
hapmaprs138761187
1000 genomesrs138761187
hgdprs138761187
ensemblrs138761187
gopubmedrs138761187
geneviewrs138761187
scholarrs138761187
googlers138761187
pharmgkbrs138761187
gwascentralrs138761187
openSNPrs138761187
23andMers138761187
23andMe allrs138761187
SNP Nexus

SNPshotrs138761187
SNPdbers138761187
MSV3drs138761187
GWAS Ctlgrs138761187
Max Magnitude0
ClinVar
Risk rs138761187(A;A)
Alt rs138761187(A;A)
Reference rs138761187(G;G)
Significance Pathogenic
Disease Premature ovarian failure 10
Variation info
Gene MCM8
CLNDBN Premature ovarian failure 10
Reversed 0
HGVS NC_000020.10:g.5966567G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190838.4,