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rs587782537

From SNPedia

Orientationplus
Geno Mag Summary
(AGAA;AGAA) 0 common in clinvar
Make rs587782537(-;-)
Make rs587782537(-;AGAA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412443
GeneMSH2
is asnp
is mentioned by
dbSNPrs587782537
ebirs587782537
HLIrs587782537
Exacrs587782537
Varsomers587782537
Maprs587782537
PheGenIrs587782537
hapmaprs587782537
1000 genomesrs587782537
hgdprs587782537
ensemblrs587782537
gopubmedrs587782537
geneviewrs587782537
scholarrs587782537
googlers587782537
pharmgkbrs587782537
gwascentralrs587782537
openSNPrs587782537
23andMers587782537
23andMe allrs587782537
SNP Nexus

SNPshotrs587782537
SNPdbers587782537
MSV3drs587782537
GWAS Ctlgrs587782537
Max Magnitude0
ClinVar
Risk rs587782537(;)
Alt rs587782537(;)
Reference rs587782537(AGAA;AGAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47639582_47639585delAGAA
CLNSRC
CLNACC RCV000131741.2,