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rs587780183

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780183(-;-)
Make rs587780183(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28725062
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780183
ebirs587780183
HLIrs587780183
Exacrs587780183
Varsomers587780183
Maprs587780183
PheGenIrs587780183
hapmaprs587780183
1000 genomesrs587780183
hgdprs587780183
ensemblrs587780183
gopubmedrs587780183
geneviewrs587780183
scholarrs587780183
googlers587780183
pharmgkbrs587780183
gwascentralrs587780183
openSNPrs587780183
23andMers587780183
23andMe allrs587780183
SNP Nexus

SNPshotrs587780183
SNPdbers587780183
MSV3drs587780183
GWAS Ctlgrs587780183
Max Magnitude0
ClinVar
Risk rs587780183(;)
Alt rs587780183(;)
Reference rs587780183(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29121050delA
CLNSRC
CLNACC RCV000116022.4,