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rs267607845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607845(A;A)
Make rs267607845(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042267
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607845
ebirs267607845
HLIrs267607845
Exacrs267607845
Varsomers267607845
Maprs267607845
PheGenIrs267607845
hapmaprs267607845
1000 genomesrs267607845
hgdprs267607845
ensemblrs267607845
gopubmedrs267607845
geneviewrs267607845
scholarrs267607845
googlers267607845
pharmgkbrs267607845
gwascentralrs267607845
openSNPrs267607845
23andMers267607845
23andMe allrs267607845
SNP Nexus

SNPshotrs267607845
SNPdbers267607845
MSV3drs267607845
GWAS Ctlgrs267607845
Max Magnitude0
ClinVar
Risk rs267607845(A,T;A,T)
Alt rs267607845(A,T;A,T)
Reference rs267607845(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.37083758G>A; NC_000003.11:g.37083758G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075300.2, RCV000214110.1, RCV000075301.2,