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rs121912960

From SNPedia

Merged intors63751612
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912960(A;G)
Make rs121912960(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047520
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912960
ClinGenrs121912960
ebirs121912960
HLIrs121912960
Exacrs121912960
Varsomers121912960
Maprs121912960
PheGenIrs121912960
hapmaprs121912960
1000 genomesrs121912960
hgdprs121912960
ensemblrs121912960
gopubmedrs121912960
geneviewrs121912960
scholarrs121912960
googlers121912960
pharmgkbrs121912960
gwascentralrs121912960
openSNPrs121912960
23andMers121912960
23andMe allrs121912960
SNP Nexus

SNPshotrs121912960
SNPdbers121912960
MSV3drs121912960
GWAS Ctlgrs121912960
StatusMerged into rs63751612
Max Magnitude0
OMIM120436
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121912960(G;G)
Alt rs121912960(G;G)
Reference Rs121912960(A;A)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37089011A>G
CLNSRC OMIM Allelic Variant
CLNACC SCV000038904.1,