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rs267607914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607914(A;A)
Make rs267607914(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408400
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607914
ebirs267607914
HLIrs267607914
Exacrs267607914
Varsomers267607914
Maprs267607914
PheGenIrs267607914
hapmaprs267607914
1000 genomesrs267607914
hgdprs267607914
ensemblrs267607914
gopubmedrs267607914
geneviewrs267607914
scholarrs267607914
googlers267607914
pharmgkbrs267607914
gwascentralrs267607914
openSNPrs267607914
23andMers267607914
23andMe allrs267607914
SNP Nexus

SNPshotrs267607914
SNPdbers267607914
MSV3drs267607914
GWAS Ctlgrs267607914
Max Magnitude0
ClinVar
Risk rs267607914(A;A)
Alt rs267607914(A;A)
Reference rs267607914(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47635539G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076394.2, RCV000202270.1, RCV000218216.1,