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rs587781531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781531(-;-)
Make rs587781531(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47471000
GeneMSH2
is asnp
is mentioned by
dbSNPrs587781531
ClinGenrs587781531
ebirs587781531
HLIrs587781531
Exacrs587781531
Varsomers587781531
Maprs587781531
PheGenIrs587781531
hapmaprs587781531
1000 genomesrs587781531
hgdprs587781531
ensemblrs587781531
gopubmedrs587781531
geneviewrs587781531
scholarrs587781531
googlers587781531
pharmgkbrs587781531
gwascentralrs587781531
openSNPrs587781531
23andMers587781531
23andMe allrs587781531
SNP Nexus

SNPshotrs587781531
SNPdbers587781531
MSV3drs587781531
GWAS Ctlgrs587781531
Max Magnitude0
ClinVar
Risk rs587781531(-;-)
Alt rs587781531(-;-)
Reference Rs587781531(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47698139delA
CLNSRC
CLNACC RCV000129525.3,