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rs267607837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607837(A;A)
Make rs267607837(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040185
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607837
ebirs267607837
HLIrs267607837
Exacrs267607837
Varsomers267607837
Maprs267607837
PheGenIrs267607837
hapmaprs267607837
1000 genomesrs267607837
hgdprs267607837
ensemblrs267607837
gopubmedrs267607837
geneviewrs267607837
scholarrs267607837
googlers267607837
pharmgkbrs267607837
gwascentralrs267607837
openSNPrs267607837
23andMers267607837
23andMe allrs267607837
SNP Nexus

SNPshotrs267607837
SNPdbers267607837
MSV3drs267607837
GWAS Ctlgrs267607837
Max Magnitude0
ClinVar
Risk rs267607837(A,C,T;A,C,T)
Alt rs267607837(A,C,T;A,C,T)
Reference rs267607837(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081676G>A; NC_000003.11:g.37081676G>C; NC_000003.11:g.37081676G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075253.2, RCV000075254.2, RCV000075255.2,