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rs587782561

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782561(-;-)
Make rs587782561(-;TTCT)
Make rs587782561(TTCT;TTCT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403314
GeneMSH2
is asnp
is mentioned by
dbSNPrs587782561
ebirs587782561
HLIrs587782561
Exacrs587782561
Varsomers587782561
Maprs587782561
PheGenIrs587782561
hapmaprs587782561
1000 genomesrs587782561
hgdprs587782561
ensemblrs587782561
gopubmedrs587782561
geneviewrs587782561
scholarrs587782561
googlers587782561
pharmgkbrs587782561
gwascentralrs587782561
openSNPrs587782561
23andMers587782561
23andMe allrs587782561
SNP Nexus

SNPshotrs587782561
SNPdbers587782561
MSV3drs587782561
GWAS Ctlgrs587782561
Max Magnitude0
ClinVar
Risk rs587782561(TTCT;TTCT)
Alt rs587782561(TTCT;TTCT)
Reference rs587782561(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47630453_47630454insTTCT
CLNSRC
CLNACC RCV000131782.2,