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rs587780173

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780173(-;-)
Make rs587780173(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28695715
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780173
ebirs587780173
HLIrs587780173
Exacrs587780173
Varsomers587780173
Maprs587780173
PheGenIrs587780173
hapmaprs587780173
1000 genomesrs587780173
hgdprs587780173
ensemblrs587780173
gopubmedrs587780173
geneviewrs587780173
scholarrs587780173
googlers587780173
pharmgkbrs587780173
gwascentralrs587780173
openSNPrs587780173
23andMers587780173
23andMe allrs587780173
SNP Nexus

SNPshotrs587780173
SNPdbers587780173
MSV3drs587780173
GWAS Ctlgrs587780173
Max Magnitude0
ClinVar
Risk rs587780173(;)
Alt rs587780173(;)
Reference rs587780173(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.29091703delA
CLNSRC
CLNACC RCV000115991.2,