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rs267607856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607856(G;G)
Make rs267607856(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042333
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607856
ebirs267607856
HLIrs267607856
Exacrs267607856
Varsomers267607856
Maprs267607856
PheGenIrs267607856
hapmaprs267607856
1000 genomesrs267607856
hgdprs267607856
ensemblrs267607856
gopubmedrs267607856
geneviewrs267607856
scholarrs267607856
googlers267607856
pharmgkbrs267607856
gwascentralrs267607856
openSNPrs267607856
23andMers267607856
23andMe allrs267607856
SNP Nexus

SNPshotrs267607856
SNPdbers267607856
MSV3drs267607856
GWAS Ctlgrs267607856
Max Magnitude0
ClinVar
Risk rs267607856(G;G)
Alt rs267607856(G;G)
Reference rs267607856(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083824T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075326.2,