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rs267607791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607791(-;-)
Make rs267607791(-;T)
Make rs267607791(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014546
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607791
ebirs267607791
HLIrs267607791
Exacrs267607791
Varsomers267607791
Maprs267607791
PheGenIrs267607791
hapmaprs267607791
1000 genomesrs267607791
hgdprs267607791
ensemblrs267607791
gopubmedrs267607791
geneviewrs267607791
scholarrs267607791
googlers267607791
pharmgkbrs267607791
gwascentralrs267607791
openSNPrs267607791
23andMers267607791
23andMe allrs267607791
SNP Nexus

SNPshotrs267607791
SNPdbers267607791
MSV3drs267607791
GWAS Ctlgrs267607791
Max Magnitude0
ClinVar
Risk rs267607791(T;T)
Alt rs267607791(T;T)
Reference rs267607791(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37056037dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075852.2,