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rs587782245

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782245(-;-)
Make rs587782245(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28724978
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782245
ebirs587782245
HLIrs587782245
Exacrs587782245
Varsomers587782245
Maprs587782245
PheGenIrs587782245
hapmaprs587782245
1000 genomesrs587782245
hgdprs587782245
ensemblrs587782245
gopubmedrs587782245
geneviewrs587782245
scholarrs587782245
googlers587782245
pharmgkbrs587782245
gwascentralrs587782245
openSNPrs587782245
23andMers587782245
23andMe allrs587782245
SNP Nexus

SNPshotrs587782245
SNPdbers587782245
MSV3drs587782245
GWAS Ctlgrs587782245
Max Magnitude0
ClinVar
Risk rs587782245(;)
Alt rs587782245(;)
Reference rs587782245(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 1
HGVS NC_000022.10:g.29120966delT
CLNSRC
CLNACC RCV000130949.4, RCV000204563.1, RCV000235159.1,