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rs267607836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607836(A;C)
Make rs267607836(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040184
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607836
ebirs267607836
HLIrs267607836
Exacrs267607836
Varsomers267607836
Maprs267607836
PheGenIrs267607836
hapmaprs267607836
1000 genomesrs267607836
hgdprs267607836
ensemblrs267607836
gopubmedrs267607836
geneviewrs267607836
scholarrs267607836
googlers267607836
pharmgkbrs267607836
gwascentralrs267607836
openSNPrs267607836
23andMers267607836
23andMe allrs267607836
SNP Nexus

SNPshotrs267607836
SNPdbers267607836
MSV3drs267607836
GWAS Ctlgrs267607836
Max Magnitude0
ClinVar
Risk rs267607836(C,G,T;C,G,T)
Alt rs267607836(C,G,T;C,G,T)
Reference rs267607836(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081675A>C; NC_000003.11:g.37081675A>G; NC_000003.11:g.37081675A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075256.2, RCV000075257.2, RCV000075258.2,