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rs587782408

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782408(C;C)
Make rs587782408(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412562
GeneMSH2
is asnp
is mentioned by
dbSNPrs587782408
ebirs587782408
HLIrs587782408
Exacrs587782408
Varsomers587782408
Maprs587782408
PheGenIrs587782408
hapmaprs587782408
1000 genomesrs587782408
hgdprs587782408
ensemblrs587782408
gopubmedrs587782408
geneviewrs587782408
scholarrs587782408
googlers587782408
pharmgkbrs587782408
gwascentralrs587782408
openSNPrs587782408
23andMers587782408
23andMe allrs587782408
SNP Nexus

SNPshotrs587782408
SNPdbers587782408
MSV3drs587782408
GWAS Ctlgrs587782408
Max Magnitude0
ClinVar
Risk rs587782408(C;C)
Alt rs587782408(C;C)
Reference rs587782408(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47639701T>C
CLNSRC
CLNACC RCV000131446.2,