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rs267608024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608024(G;T)
Make rs267608024(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47482884
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608024
ebirs267608024
HLIrs267608024
Exacrs267608024
Varsomers267608024
Maprs267608024
PheGenIrs267608024
hapmaprs267608024
1000 genomesrs267608024
hgdprs267608024
ensemblrs267608024
gopubmedrs267608024
geneviewrs267608024
scholarrs267608024
googlers267608024
pharmgkbrs267608024
gwascentralrs267608024
openSNPrs267608024
23andMers267608024
23andMe allrs267608024
SNP Nexus

SNPshotrs267608024
SNPdbers267608024
MSV3drs267608024
GWAS Ctlgrs267608024
Max Magnitude0
ClinVar
Risk rs267608024(T;T)
Alt rs267608024(T;T)
Reference rs267608024(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47710023G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076542.2,