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rs267607894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607894(C;C)
Make rs267607894(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050628
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607894
ebirs267607894
HLIrs267607894
Exacrs267607894
Varsomers267607894
Maprs267607894
PheGenIrs267607894
hapmaprs267607894
1000 genomesrs267607894
hgdprs267607894
ensemblrs267607894
gopubmedrs267607894
geneviewrs267607894
scholarrs267607894
googlers267607894
pharmgkbrs267607894
gwascentralrs267607894
openSNPrs267607894
23andMers267607894
23andMe allrs267607894
SNP Nexus

SNPshotrs267607894
SNPdbers267607894
MSV3drs267607894
GWAS Ctlgrs267607894
Max Magnitude0
ClinVar
Risk rs267607894(A,C;A,C)
Alt rs267607894(A,C;A,C)
Reference rs267607894(T;T)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37092119T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075583.2, RCV000216146.1,