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rs587781699

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781699(A;A)
Make rs587781699(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28703504
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587781699
ebirs587781699
HLIrs587781699
Exacrs587781699
Varsomers587781699
Maprs587781699
PheGenIrs587781699
hapmaprs587781699
1000 genomesrs587781699
hgdprs587781699
ensemblrs587781699
gopubmedrs587781699
geneviewrs587781699
scholarrs587781699
googlers587781699
pharmgkbrs587781699
gwascentralrs587781699
openSNPrs587781699
23andMers587781699
23andMe allrs587781699
SNP Nexus

SNPshotrs587781699
SNPdbers587781699
MSV3drs587781699
GWAS Ctlgrs587781699
Max Magnitude0
ClinVar
Risk rs587781699(A;A)
Alt rs587781699(A;A)
Reference rs587781699(G;G)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29099492C>A; NC_000022.10:g.29099492C>T
CLNSRC
CLNACC RCV000219083.1, RCV000129866.2,