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rs587781836

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781836(A;A)
Make rs587781836(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28695757
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587781836
ebirs587781836
HLIrs587781836
Exacrs587781836
Varsomers587781836
Maprs587781836
PheGenIrs587781836
hapmaprs587781836
1000 genomesrs587781836
hgdprs587781836
ensemblrs587781836
gopubmedrs587781836
geneviewrs587781836
scholarrs587781836
googlers587781836
pharmgkbrs587781836
gwascentralrs587781836
openSNPrs587781836
23andMers587781836
23andMe allrs587781836
SNP Nexus

SNPshotrs587781836
SNPdbers587781836
MSV3drs587781836
GWAS Ctlgrs587781836
Max Magnitude0
ClinVar
Risk rs587781836(A;A)
Alt rs587781836(A;A)
Reference rs587781836(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.29091745A>T
CLNSRC
CLNACC RCV000130129.2,