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rs267607777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607777(A;G)
Make rs267607777(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017603
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607777
ebirs267607777
HLIrs267607777
Exacrs267607777
Varsomers267607777
Maprs267607777
PheGenIrs267607777
hapmaprs267607777
1000 genomesrs267607777
hgdprs267607777
ensemblrs267607777
gopubmedrs267607777
geneviewrs267607777
scholarrs267607777
googlers267607777
pharmgkbrs267607777
gwascentralrs267607777
openSNPrs267607777
23andMers267607777
23andMe allrs267607777
SNP Nexus

SNPshotrs267607777
SNPdbers267607777
MSV3drs267607777
GWAS Ctlgrs267607777
Max Magnitude0
ClinVar
Risk rs267607777(G;G)
Alt rs267607777(G;G)
Reference rs267607777(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059094A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075907.2,