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rs267607794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607794(A;G)
Make rs267607794(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017504
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607794
ebirs267607794
HLIrs267607794
Exacrs267607794
Varsomers267607794
Maprs267607794
PheGenIrs267607794
hapmaprs267607794
1000 genomesrs267607794
hgdprs267607794
ensemblrs267607794
gopubmedrs267607794
geneviewrs267607794
scholarrs267607794
googlers267607794
pharmgkbrs267607794
gwascentralrs267607794
openSNPrs267607794
23andMers267607794
23andMe allrs267607794
SNP Nexus

SNPshotrs267607794
SNPdbers267607794
MSV3drs267607794
GWAS Ctlgrs267607794
Max Magnitude0
ClinVar
Risk rs267607794(G;G)
Alt rs267607794(G;G)
Reference rs267607794(A;A)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37058995A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075863.2, RCV000115486.4, RCV000212525.1,