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rs587782830

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782830(C;C)
Make rs587782830(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28725125
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782830
ebirs587782830
HLIrs587782830
Exacrs587782830
Varsomers587782830
Maprs587782830
PheGenIrs587782830
hapmaprs587782830
1000 genomesrs587782830
hgdprs587782830
ensemblrs587782830
gopubmedrs587782830
geneviewrs587782830
scholarrs587782830
googlers587782830
pharmgkbrs587782830
gwascentralrs587782830
openSNPrs587782830
23andMers587782830
23andMe allrs587782830
SNP Nexus

SNPshotrs587782830
SNPdbers587782830
MSV3drs587782830
GWAS Ctlgrs587782830
Max Magnitude0
ClinVar
Risk rs587782830(C;C)
Alt rs587782830(C;C)
Reference rs587782830(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29121113C>G
CLNSRC
CLNACC RCV000132412.2,