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rs587782684

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782684(-;-)
Make rs587782684(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28687962
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782684
ebirs587782684
HLIrs587782684
Exacrs587782684
Varsomers587782684
Maprs587782684
PheGenIrs587782684
hapmaprs587782684
1000 genomesrs587782684
hgdprs587782684
ensemblrs587782684
gopubmedrs587782684
geneviewrs587782684
scholarrs587782684
googlers587782684
pharmgkbrs587782684
gwascentralrs587782684
openSNPrs587782684
23andMers587782684
23andMe allrs587782684
SNP Nexus

SNPshotrs587782684
SNPdbers587782684
MSV3drs587782684
GWAS Ctlgrs587782684
Max Magnitude0
ClinVar
Risk rs587782684(;)
Alt rs587782684(;)
Reference rs587782684(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Reversed 1
HGVS NC_000022.10:g.29083950delG
CLNSRC
CLNACC RCV000132111.5, RCV000205272.1, RCV000212478.1,