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rs121912957

From SNPedia

Merged intors63751109
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912957(C;T)
Make rs121912957(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996633
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912957
ebirs121912957
HLIrs121912957
Exacrs121912957
Varsomers121912957
Maprs121912957
PheGenIrs121912957
hapmaprs121912957
1000 genomesrs121912957
hgdprs121912957
ensemblrs121912957
gopubmedrs121912957
geneviewrs121912957
scholarrs121912957
googlers121912957
pharmgkbrs121912957
gwascentralrs121912957
openSNPrs121912957
23andMers121912957
23andMe allrs121912957
SNP Nexus

SNPshotrs121912957
SNPdbers121912957
MSV3drs121912957
GWAS Ctlgrs121912957
StatusMerged into rs63751109
Max Magnitude0
OMIM120436
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912957(T;T)
Alt rs121912957(T;T)
Reference rs121912957(C;C)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37038124C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000038891.1,