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

rs587782529

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782529(C;T)
Make rs587782529(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7670700
GeneTP53
is asnp
is mentioned by
dbSNPrs587782529
ebirs587782529
HLIrs587782529
Exacrs587782529
Varsomers587782529
Maprs587782529
PheGenIrs587782529
hapmaprs587782529
1000 genomesrs587782529
hgdprs587782529
ensemblrs587782529
gopubmedrs587782529
geneviewrs587782529
scholarrs587782529
googlers587782529
pharmgkbrs587782529
gwascentralrs587782529
openSNPrs587782529
23andMers587782529
23andMe allrs587782529
SNP Nexus

SNPshotrs587782529
SNPdbers587782529
MSV3drs587782529
GWAS Ctlgrs587782529
Max Magnitude0
ClinVar
Risk rs587782529(G,T;G,T)
Alt rs587782529(G,T;G,T)
Reference rs587782529(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7574018G>A; NC_000017.10:g.7574018G>C
CLNSRC
CLNACC RCV000131726.2, RCV000226515.1,