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rs267607832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607832(G;T)
Make rs267607832(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028933
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607832
ebirs267607832
HLIrs267607832
Exacrs267607832
Varsomers267607832
Maprs267607832
PheGenIrs267607832
hapmaprs267607832
1000 genomesrs267607832
hgdprs267607832
ensemblrs267607832
gopubmedrs267607832
geneviewrs267607832
scholarrs267607832
googlers267607832
pharmgkbrs267607832
gwascentralrs267607832
openSNPrs267607832
23andMers267607832
23andMe allrs267607832
SNP Nexus

SNPshotrs267607832
SNPdbers267607832
MSV3drs267607832
GWAS Ctlgrs267607832
Max Magnitude0
ClinVar
Risk rs267607832(T;T)
Alt rs267607832(T;T)
Reference rs267607832(G;G)
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.37070424G>A; NC_000003.11:g.37070424G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000204627.1, RCV000223493.1, RCV000075246.2,