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rs587782575

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782575(A;G)
Make rs587782575(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28689217
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782575
ebirs587782575
HLIrs587782575
Exacrs587782575
Varsomers587782575
Maprs587782575
PheGenIrs587782575
hapmaprs587782575
1000 genomesrs587782575
hgdprs587782575
ensemblrs587782575
gopubmedrs587782575
geneviewrs587782575
scholarrs587782575
googlers587782575
pharmgkbrs587782575
gwascentralrs587782575
openSNPrs587782575
23andMers587782575
23andMe allrs587782575
SNP Nexus

SNPshotrs587782575
SNPdbers587782575
MSV3drs587782575
GWAS Ctlgrs587782575
Max Magnitude0
ClinVar
Risk rs587782575(G;G)
Alt rs587782575(G;G)
Reference rs587782575(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29085205T>C
CLNSRC
CLNACC RCV000131803.2,