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rs587780184

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780184(-;-)
Make rs587780184(-;T)
Make rs587780184(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28725044
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780184
ebirs587780184
HLIrs587780184
Exacrs587780184
Varsomers587780184
Maprs587780184
PheGenIrs587780184
hapmaprs587780184
1000 genomesrs587780184
hgdprs587780184
ensemblrs587780184
gopubmedrs587780184
geneviewrs587780184
scholarrs587780184
googlers587780184
pharmgkbrs587780184
gwascentralrs587780184
openSNPrs587780184
23andMers587780184
23andMe allrs587780184
SNP Nexus

SNPshotrs587780184
SNPdbers587780184
MSV3drs587780184
GWAS Ctlgrs587780184
Max Magnitude0
ClinVar
Risk rs587780184(T;T)
Alt rs587780184(T;T)
Reference rs587780184(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000022.10:g.29121033dupA
CLNSRC
CLNACC RCV000116023.2, RCV000220798.1,