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rs587782070

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782070(A;A)
Make rs587782070(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734443
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587782070
ebirs587782070
HLIrs587782070
Exacrs587782070
Varsomers587782070
Maprs587782070
PheGenIrs587782070
hapmaprs587782070
1000 genomesrs587782070
hgdprs587782070
ensemblrs587782070
gopubmedrs587782070
geneviewrs587782070
scholarrs587782070
googlers587782070
pharmgkbrs587782070
gwascentralrs587782070
openSNPrs587782070
23andMers587782070
23andMe allrs587782070
SNP Nexus

SNPshotrs587782070
SNPdbers587782070
MSV3drs587782070
GWAS Ctlgrs587782070
Max Magnitude0
ClinVar
Risk rs587782070(A;A)
Alt rs587782070(A;A)
Reference rs587782070(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29130431C>T
CLNSRC
CLNACC RCV000130559.2, RCV000199638.2,