Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781564

From SNPedia

Orientationminus
Geno Mag Summary
(AGAGACCGGCG;AGAGACCGGCG) 0 common in clinvar
Make rs587781564(AGAGACCGGCG;CA)
Make rs587781564(CA;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673772
GeneTP53
is asnp
is mentioned by
dbSNPrs587781564
ebirs587781564
HLIrs587781564
Exacrs587781564
Varsomers587781564
Maprs587781564
PheGenIrs587781564
hapmaprs587781564
1000 genomesrs587781564
hgdprs587781564
ensemblrs587781564
gopubmedrs587781564
geneviewrs587781564
scholarrs587781564
googlers587781564
pharmgkbrs587781564
gwascentralrs587781564
openSNPrs587781564
23andMers587781564
23andMe allrs587781564
SNP Nexus

SNPshotrs587781564
SNPdbers587781564
MSV3drs587781564
GWAS Ctlgrs587781564
Max Magnitude0
ClinVar
Risk rs587781564(CA;CA)
Alt rs587781564(CA;CA)
Reference rs587781564(AGAGACCGGCG;AGAGACCGGCG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577090_7577100delCGCCGGTCTCTinsTG
CLNSRC
CLNACC RCV000129588.2,