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rs267607884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607884(C;T)
Make rs267607884(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048903
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607884
ebirs267607884
HLIrs267607884
Exacrs267607884
Varsomers267607884
Maprs267607884
PheGenIrs267607884
hapmaprs267607884
1000 genomesrs267607884
hgdprs267607884
ensemblrs267607884
gopubmedrs267607884
geneviewrs267607884
scholarrs267607884
googlers267607884
pharmgkbrs267607884
gwascentralrs267607884
openSNPrs267607884
23andMers267607884
23andMe allrs267607884
SNP Nexus

SNPshotrs267607884
SNPdbers267607884
MSV3drs267607884
GWAS Ctlgrs267607884
Max Magnitude0
ClinVar
Risk rs267607884(A,T;A,T)
Alt rs267607884(A,T;A,T)
Reference rs267607884(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000003.11:g.37090394G>A; NC_000003.11:g.37090394G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075467.2, RCV000075468.2,