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rs267607943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607943(A;C)
Make rs267607943(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429740
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607943
ebirs267607943
HLIrs267607943
Exacrs267607943
Varsomers267607943
Maprs267607943
PheGenIrs267607943
hapmaprs267607943
1000 genomesrs267607943
hgdprs267607943
ensemblrs267607943
gopubmedrs267607943
geneviewrs267607943
scholarrs267607943
googlers267607943
pharmgkbrs267607943
gwascentralrs267607943
openSNPrs267607943
23andMers267607943
23andMe allrs267607943
SNP Nexus

SNPshotrs267607943
SNPdbers267607943
MSV3drs267607943
GWAS Ctlgrs267607943
Max Magnitude0
ClinVar
Risk rs267607943(C,G,T;C,G,T)
Alt rs267607943(C,G,T;C,G,T)
Reference rs267607943(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656879A>C; NC_000002.11:g.47656879A>G; NC_000002.11:g.47656879A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076023.2, RCV000076024.2, RCV000076025.2,