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rs267607957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607957(G;T)
Make rs267607957(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445658
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607957
ebirs267607957
HLIrs267607957
Exacrs267607957
Varsomers267607957
Maprs267607957
PheGenIrs267607957
hapmaprs267607957
1000 genomesrs267607957
hgdprs267607957
ensemblrs267607957
gopubmedrs267607957
geneviewrs267607957
scholarrs267607957
googlers267607957
pharmgkbrs267607957
gwascentralrs267607957
openSNPrs267607957
23andMers267607957
23andMe allrs267607957
SNP Nexus

SNPshotrs267607957
SNPdbers267607957
MSV3drs267607957
GWAS Ctlgrs267607957
Max Magnitude0
ClinVar
Risk rs267607957(A,C,T;A,C,T)
Alt rs267607957(A,C,T;A,C,T)
Reference rs267607957(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672797G>A; NC_000002.11:g.47672797G>C; NC_000002.11:g.47672797G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076137.3, RCV000076138.2, RCV000076139.2,