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

rs267607798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607798(-;-)
Make rs267607798(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014545
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607798
ebirs267607798
HLIrs267607798
Exacrs267607798
Varsomers267607798
Maprs267607798
PheGenIrs267607798
hapmaprs267607798
1000 genomesrs267607798
hgdprs267607798
ensemblrs267607798
gopubmedrs267607798
geneviewrs267607798
scholarrs267607798
googlers267607798
pharmgkbrs267607798
gwascentralrs267607798
openSNPrs267607798
23andMers267607798
23andMe allrs267607798
SNP Nexus

SNPshotrs267607798
SNPdbers267607798
MSV3drs267607798
GWAS Ctlgrs267607798
Max Magnitude0
ClinVar
Risk rs267607798(;)
Alt rs267607798(;)
Reference rs267607798(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37056036delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075849.2,