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rs121912961

From SNPedia

Merged intors63750781
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912961(C;T)
Make rs121912961(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004444
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912961
ebirs121912961
HLIrs121912961
Exacrs121912961
Varsomers121912961
Maprs121912961
PheGenIrs121912961
hapmaprs121912961
1000 genomesrs121912961
hgdprs121912961
ensemblrs121912961
gopubmedrs121912961
geneviewrs121912961
scholarrs121912961
googlers121912961
pharmgkbrs121912961
gwascentralrs121912961
openSNPrs121912961
23andMers121912961
23andMe allrs121912961
SNP Nexus

SNPshotrs121912961
SNPdbers121912961
MSV3drs121912961
GWAS Ctlgrs121912961
StatusMerged into rs63750781
Max Magnitude0
OMIM120436
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121912961(T;T)
Alt rs121912961(T;T)
Reference rs121912961(C;C)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37045935C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000038909.1,