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rs267607772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607772(G;T)
Make rs267607772(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011863
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607772
ebirs267607772
HLIrs267607772
Exacrs267607772
Varsomers267607772
Maprs267607772
PheGenIrs267607772
hapmaprs267607772
1000 genomesrs267607772
hgdprs267607772
ensemblrs267607772
gopubmedrs267607772
geneviewrs267607772
scholarrs267607772
googlers267607772
pharmgkbrs267607772
gwascentralrs267607772
openSNPrs267607772
23andMers267607772
23andMe allrs267607772
SNP Nexus

SNPshotrs267607772
SNPdbers267607772
MSV3drs267607772
GWAS Ctlgrs267607772
Max Magnitude0
ClinVar
Risk rs267607772(T;T)
Alt rs267607772(T;T)
Reference rs267607772(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053354G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075769.2,