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rs267607780

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607780(G;G)
Make rs267607780(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012102
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607780
ebirs267607780
HLIrs267607780
Exacrs267607780
Varsomers267607780
Maprs267607780
PheGenIrs267607780
hapmaprs267607780
1000 genomesrs267607780
hgdprs267607780
ensemblrs267607780
gopubmedrs267607780
geneviewrs267607780
scholarrs267607780
googlers267607780
pharmgkbrs267607780
gwascentralrs267607780
openSNPrs267607780
23andMers267607780
23andMe allrs267607780
SNP Nexus

SNPshotrs267607780
SNPdbers267607780
MSV3drs267607780
GWAS Ctlgrs267607780
Max Magnitude0
ClinVar
Risk rs267607780(C,G;C,G)
Alt rs267607780(C,G;C,G)
Reference rs267607780(T;T)
Significance Pathogenic
Disease Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000003.11:g.37053593A>C; NC_000003.11:g.37053593A>G; NC_000003.11:g.37053593A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075805.2, RCV000075806.2, RCV000201996.1, RCV000222833.1, RCV000215214.1,