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rs121912956

From SNPedia

Merged intors63750198
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912956(A;A)
Make rs121912956(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014509
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912956
ebirs121912956
HLIrs121912956
Exacrs121912956
Varsomers121912956
Maprs121912956
PheGenIrs121912956
hapmaprs121912956
1000 genomesrs121912956
hgdprs121912956
ensemblrs121912956
gopubmedrs121912956
geneviewrs121912956
scholarrs121912956
googlers121912956
pharmgkbrs121912956
gwascentralrs121912956
openSNPrs121912956
23andMers121912956
23andMe allrs121912956
SNP Nexus

SNPshotrs121912956
SNPdbers121912956
MSV3drs121912956
GWAS Ctlgrs121912956
StatusMerged into rs63750198
Max Magnitude0
OMIM120436
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912956(A;A)
Alt rs121912956(A;A)
Reference rs121912956(C;C)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37056000C>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000038890.1,