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rs587782766

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782766(-;-)
Make rs587782766(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734475
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782766
ebirs587782766
HLIrs587782766
Exacrs587782766
Varsomers587782766
Maprs587782766
PheGenIrs587782766
hapmaprs587782766
1000 genomesrs587782766
hgdprs587782766
ensemblrs587782766
gopubmedrs587782766
geneviewrs587782766
scholarrs587782766
googlers587782766
pharmgkbrs587782766
gwascentralrs587782766
openSNPrs587782766
23andMers587782766
23andMe allrs587782766
SNP Nexus

SNPshotrs587782766
SNPdbers587782766
MSV3drs587782766
GWAS Ctlgrs587782766
Max Magnitude0
ClinVar
Risk rs587782766(;)
Alt rs587782766(;)
Reference rs587782766(C;C)
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.29130463delG
CLNSRC
CLNACC RCV000132293.2, RCV000204969.2, RCV000220709.1,