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rs587779163

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779163(G;G)
Make rs587779163(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47410220
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779163
ebirs587779163
HLIrs587779163
Exacrs587779163
Varsomers587779163
Maprs587779163
PheGenIrs587779163
hapmaprs587779163
1000 genomesrs587779163
hgdprs587779163
ensemblrs587779163
gopubmedrs587779163
geneviewrs587779163
scholarrs587779163
googlers587779163
pharmgkbrs587779163
gwascentralrs587779163
openSNPrs587779163
23andMers587779163
23andMe allrs587779163
SNP Nexus

SNPshotrs587779163
SNPdbers587779163
MSV3drs587779163
GWAS Ctlgrs587779163
Max Magnitude0
ClinVar
Risk rs587779163(G;G)
Alt rs587779163(G;G)
Reference rs587779163(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637359T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076614.3,