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rs587782659

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782659(C;C)
Make rs587782659(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403402
GeneMSH2
is asnp
is mentioned by
dbSNPrs587782659
ebirs587782659
HLIrs587782659
Exacrs587782659
Varsomers587782659
Maprs587782659
PheGenIrs587782659
hapmaprs587782659
1000 genomesrs587782659
hgdprs587782659
ensemblrs587782659
gopubmedrs587782659
geneviewrs587782659
scholarrs587782659
googlers587782659
pharmgkbrs587782659
gwascentralrs587782659
openSNPrs587782659
23andMers587782659
23andMe allrs587782659
SNP Nexus

SNPshotrs587782659
SNPdbers587782659
MSV3drs587782659
GWAS Ctlgrs587782659
Max Magnitude0
ClinVar
Risk rs587782659(C;C)
Alt rs587782659(C;C)
Reference rs587782659(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47630541G>C
CLNSRC
CLNACC RCV000132075.2,