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rs267607753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607753(A;G)
Make rs267607753(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008812
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607753
ebirs267607753
HLIrs267607753
Exacrs267607753
Varsomers267607753
Maprs267607753
PheGenIrs267607753
hapmaprs267607753
1000 genomesrs267607753
hgdprs267607753
ensemblrs267607753
gopubmedrs267607753
geneviewrs267607753
scholarrs267607753
googlers267607753
pharmgkbrs267607753
gwascentralrs267607753
openSNPrs267607753
23andMers267607753
23andMe allrs267607753
SNP Nexus

SNPshotrs267607753
SNPdbers267607753
MSV3drs267607753
GWAS Ctlgrs267607753
Max Magnitude0
ClinVar
Risk rs267607753(G;G)
Alt rs267607753(G;G)
Reference rs267607753(A;A)
Significance Probable-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.37050303A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075721.2, RCV000218165.1,