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rs267607991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607991(A;G)
Make rs267607991(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476365
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607991
ebirs267607991
HLIrs267607991
Exacrs267607991
Varsomers267607991
Maprs267607991
PheGenIrs267607991
hapmaprs267607991
1000 genomesrs267607991
hgdprs267607991
ensemblrs267607991
gopubmedrs267607991
geneviewrs267607991
scholarrs267607991
googlers267607991
pharmgkbrs267607991
gwascentralrs267607991
openSNPrs267607991
23andMers267607991
23andMe allrs267607991
SNP Nexus

SNPshotrs267607991
SNPdbers267607991
MSV3drs267607991
GWAS Ctlgrs267607991
Max Magnitude0
ClinVar
Risk rs267607991(G;G)
Alt rs267607991(G;G)
Reference rs267607991(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703504A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076349.2,