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rs587781592

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781592(C;T)
Make rs587781592(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734571
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587781592
ebirs587781592
HLIrs587781592
Exacrs587781592
Varsomers587781592
Maprs587781592
PheGenIrs587781592
hapmaprs587781592
1000 genomesrs587781592
hgdprs587781592
ensemblrs587781592
gopubmedrs587781592
geneviewrs587781592
scholarrs587781592
googlers587781592
pharmgkbrs587781592
gwascentralrs587781592
openSNPrs587781592
23andMers587781592
23andMe allrs587781592
SNP Nexus

SNPshotrs587781592
SNPdbers587781592
MSV3drs587781592
GWAS Ctlgrs587781592
Max Magnitude0
ClinVar
Risk rs587781592(T;T)
Alt rs587781592(T;T)
Reference rs587781592(C;C)
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.29130559G>A
CLNSRC
CLNACC RCV000129647.2, RCV000195906.1,