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rs121912966

From SNPedia

Merged intors63749939
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912966(A;A)
Make rs121912966(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996702
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912966
ebirs121912966
HLIrs121912966
Exacrs121912966
Varsomers121912966
Maprs121912966
PheGenIrs121912966
hapmaprs121912966
1000 genomesrs121912966
hgdprs121912966
ensemblrs121912966
gopubmedrs121912966
geneviewrs121912966
scholarrs121912966
googlers121912966
pharmgkbrs121912966
gwascentralrs121912966
openSNPrs121912966
23andMers121912966
23andMe allrs121912966
SNP Nexus

SNPshotrs121912966
SNPdbers121912966
MSV3drs121912966
GWAS Ctlgrs121912966
StatusMerged into rs63749939
Max Magnitude0
OMIM120436
Desc
Variant0029
Relatedalso
ClinVar
Risk rs121912966(A;A)
Alt rs121912966(A;A)
Reference rs121912966(G;G)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37038193G>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000038924.1,