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rs587779133

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779133(C;C)
Make rs587779133(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47476421
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779133
ebirs587779133
HLIrs587779133
Exacrs587779133
Varsomers587779133
Maprs587779133
PheGenIrs587779133
hapmaprs587779133
1000 genomesrs587779133
hgdprs587779133
ensemblrs587779133
gopubmedrs587779133
geneviewrs587779133
scholarrs587779133
googlers587779133
pharmgkbrs587779133
gwascentralrs587779133
openSNPrs587779133
23andMers587779133
23andMe allrs587779133
SNP Nexus

SNPshotrs587779133
SNPdbers587779133
MSV3drs587779133
GWAS Ctlgrs587779133
Max Magnitude0
ClinVar
Risk rs587779133(C;C)
Alt rs587779133(C;C)
Reference rs587779133(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47703560T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076375.2, RCV000160600.4, RCV000212614.1,