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rs121912958

From SNPedia

Merged intors63751615
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912958(C;T)
Make rs121912958(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012098
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912958
ebirs121912958
HLIrs121912958
Exacrs121912958
Varsomers121912958
Maprs121912958
PheGenIrs121912958
hapmaprs121912958
1000 genomesrs121912958
hgdprs121912958
ensemblrs121912958
gopubmedrs121912958
geneviewrs121912958
scholarrs121912958
googlers121912958
pharmgkbrs121912958
gwascentralrs121912958
openSNPrs121912958
23andMers121912958
23andMe allrs121912958
SNP Nexus

SNPshotrs121912958
SNPdbers121912958
MSV3drs121912958
GWAS Ctlgrs121912958
StatusMerged into rs63751615
Max Magnitude0
OMIM120436
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121912958(T;T)
Alt rs121912958(T;T)
Reference rs121912958(C;C)
Significance Pathogenic
Disease Lynch syndrome II Turcot syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome II Turcot syndrome
Reversed 0
HGVS NC_000003.11:g.37053589C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000038899.1, SCV000038900.1,