Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607742(A;A)
Make rs267607742(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004476
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607742
ebirs267607742
HLIrs267607742
Exacrs267607742
Varsomers267607742
Maprs267607742
PheGenIrs267607742
hapmaprs267607742
1000 genomesrs267607742
hgdprs267607742
ensemblrs267607742
gopubmedrs267607742
geneviewrs267607742
scholarrs267607742
googlers267607742
pharmgkbrs267607742
gwascentralrs267607742
openSNPrs267607742
23andMers267607742
23andMe allrs267607742
SNP Nexus

SNPshotrs267607742
SNPdbers267607742
MSV3drs267607742
GWAS Ctlgrs267607742
Max Magnitude0
ClinVar
Risk rs267607742(A,C;A,C)
Alt rs267607742(A,C;A,C)
Reference rs267607742(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045967T>A; NC_000003.11:g.37045967T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075680.2, RCV000075681.2,