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

rs267607851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607851(A;T)
Make rs267607851(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042334
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607851
ebirs267607851
HLIrs267607851
Exacrs267607851
Varsomers267607851
Maprs267607851
PheGenIrs267607851
hapmaprs267607851
1000 genomesrs267607851
hgdprs267607851
ensemblrs267607851
gopubmedrs267607851
geneviewrs267607851
scholarrs267607851
googlers267607851
pharmgkbrs267607851
gwascentralrs267607851
openSNPrs267607851
23andMers267607851
23andMe allrs267607851
SNP Nexus

SNPshotrs267607851
SNPdbers267607851
MSV3drs267607851
GWAS Ctlgrs267607851
Max Magnitude0
ClinVar
Risk rs267607851(T;T)
Alt rs267607851(T;T)
Reference rs267607851(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083825A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075327.2,