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rs267607867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607867(A;A)
Make rs267607867(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047684
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607867
ebirs267607867
HLIrs267607867
Exacrs267607867
Varsomers267607867
Maprs267607867
PheGenIrs267607867
hapmaprs267607867
1000 genomesrs267607867
hgdprs267607867
ensemblrs267607867
gopubmedrs267607867
geneviewrs267607867
scholarrs267607867
googlers267607867
pharmgkbrs267607867
gwascentralrs267607867
openSNPrs267607867
23andMers267607867
23andMe allrs267607867
SNP Nexus

SNPshotrs267607867
SNPdbers267607867
MSV3drs267607867
GWAS Ctlgrs267607867
Max Magnitude0
ClinVar
Risk rs267607867(A,T;A,T)
Alt rs267607867(A,T;A,T)
Reference rs267607867(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089175G>A; NC_000003.11:g.37089175G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075404.2, RCV000075405.2,