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rs587781705

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781705(G;G)
Make rs587781705(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734506
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587781705
ebirs587781705
HLIrs587781705
Exacrs587781705
Varsomers587781705
Maprs587781705
PheGenIrs587781705
hapmaprs587781705
1000 genomesrs587781705
hgdprs587781705
ensemblrs587781705
gopubmedrs587781705
geneviewrs587781705
scholarrs587781705
googlers587781705
pharmgkbrs587781705
gwascentralrs587781705
openSNPrs587781705
23andMers587781705
23andMe allrs587781705
SNP Nexus

SNPshotrs587781705
SNPdbers587781705
MSV3drs587781705
GWAS Ctlgrs587781705
Max Magnitude0
ClinVar
Risk rs587781705(G;G)
Alt rs587781705(G;G)
Reference rs587781705(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.29130494A>C
CLNSRC
CLNACC RCV000129876.2,