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

rs587782609

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782609(-;-)
Make rs587782609(-;AAT)
Make rs587782609(AAT;AAT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676211
GeneTP53
is asnp
is mentioned by
dbSNPrs587782609
ebirs587782609
HLIrs587782609
Exacrs587782609
Varsomers587782609
Maprs587782609
PheGenIrs587782609
hapmaprs587782609
1000 genomesrs587782609
hgdprs587782609
ensemblrs587782609
gopubmedrs587782609
geneviewrs587782609
scholarrs587782609
googlers587782609
pharmgkbrs587782609
gwascentralrs587782609
openSNPrs587782609
23andMers587782609
23andMe allrs587782609
SNP Nexus

SNPshotrs587782609
SNPdbers587782609
MSV3drs587782609
GWAS Ctlgrs587782609
Max Magnitude0
ClinVar
Risk rs587782609(AAT;AAT)
Alt rs587782609(AAT;AAT)
Reference rs587782609(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579530_7579532dupATT
CLNSRC
CLNACC RCV000131982.2,