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rs267607825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607825(C;T)
Make rs267607825(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37026008
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607825
ebirs267607825
HLIrs267607825
Exacrs267607825
Varsomers267607825
Maprs267607825
PheGenIrs267607825
hapmaprs267607825
1000 genomesrs267607825
hgdprs267607825
ensemblrs267607825
gopubmedrs267607825
geneviewrs267607825
scholarrs267607825
googlers267607825
pharmgkbrs267607825
gwascentralrs267607825
openSNPrs267607825
23andMers267607825
23andMe allrs267607825
SNP Nexus

SNPshotrs267607825
SNPdbers267607825
MSV3drs267607825
GWAS Ctlgrs267607825
Max Magnitude0
ClinVar
Risk rs267607825(G,T;G,T)
Alt rs267607825(G,T;G,T)
Reference rs267607825(C;C)
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 1
HGVS NC_000003.11:g.37067499G>A; NC_000003.11:g.37067499G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075192.2, RCV000220831.1, RCV000075193.2,