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rs587782401

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782401(A;A)
Make rs587782401(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28734401
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782401
ebirs587782401
HLIrs587782401
Exacrs587782401
Varsomers587782401
Maprs587782401
PheGenIrs587782401
hapmaprs587782401
1000 genomesrs587782401
hgdprs587782401
ensemblrs587782401
gopubmedrs587782401
geneviewrs587782401
scholarrs587782401
googlers587782401
pharmgkbrs587782401
gwascentralrs587782401
openSNPrs587782401
23andMers587782401
23andMe allrs587782401
SNP Nexus

SNPshotrs587782401
SNPdbers587782401
MSV3drs587782401
GWAS Ctlgrs587782401
Max Magnitude0
Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312OA-icon.png]
ClinVar
Risk rs587782401(A;A)
Alt rs587782401(A;A)
Reference rs587782401(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000022.10:g.29130389A>T
CLNSRC
CLNACC RCV000131434.5, RCV000212411.1,