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rs267607996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607996(C;C)
Make rs267607996(C;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position47476382
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607996
ebirs267607996
HLIrs267607996
Exacrs267607996
Varsomers267607996
Maprs267607996
PheGenIrs267607996
hapmaprs267607996
1000 genomesrs267607996
hgdprs267607996
ensemblrs267607996
gopubmedrs267607996
geneviewrs267607996
scholarrs267607996
googlers267607996
pharmgkbrs267607996
gwascentralrs267607996
openSNPrs267607996
23andMers267607996
23andMe allrs267607996
SNP Nexus

SNPshotrs267607996
SNPdbers267607996
MSV3drs267607996
GWAS Ctlgrs267607996
Max Magnitude0
ClinVar
Risk rs267607996(A,C;A,C)
Alt rs267607996(A,C;A,C)
Reference rs267607996(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703521G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076363.2,