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rs267607917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607917(A;G)
Make rs267607917(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408399
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607917
ebirs267607917
HLIrs267607917
Exacrs267607917
Varsomers267607917
Maprs267607917
PheGenIrs267607917
hapmaprs267607917
1000 genomesrs267607917
hgdprs267607917
ensemblrs267607917
gopubmedrs267607917
geneviewrs267607917
scholarrs267607917
googlers267607917
pharmgkbrs267607917
gwascentralrs267607917
openSNPrs267607917
23andMers267607917
23andMe allrs267607917
SNP Nexus

SNPshotrs267607917
SNPdbers267607917
MSV3drs267607917
GWAS Ctlgrs267607917
Max Magnitude0
ClinVar
Risk rs267607917(G;G)
Alt rs267607917(G;G)
Reference rs267607917(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635538A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076395.2,