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rs121912964

From SNPedia

Merged intors63750691
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912964(C;G)
Make rs121912964(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017521
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912964
ebirs121912964
HLIrs121912964
Exacrs121912964
Varsomers121912964
Maprs121912964
PheGenIrs121912964
hapmaprs121912964
1000 genomesrs121912964
hgdprs121912964
ensemblrs121912964
gopubmedrs121912964
geneviewrs121912964
scholarrs121912964
googlers121912964
pharmgkbrs121912964
gwascentralrs121912964
openSNPrs121912964
23andMers121912964
23andMe allrs121912964
SNP Nexus

SNPshotrs121912964
SNPdbers121912964
MSV3drs121912964
GWAS Ctlgrs121912964
StatusMerged into rs63750691
Max Magnitude0
OMIM120436
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121912964(G;G)
Alt rs121912964(G;G)
Reference rs121912964(C;C)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37059012C>G
CLNSRC OMIM Allelic Variant
CLNACC SCV000038914.1,