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

rs587780073

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780073(A;G)
Make rs587780073(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674262
GeneTP53
is asnp
is mentioned by
dbSNPrs587780073
ebirs587780073
HLIrs587780073
Exacrs587780073
Varsomers587780073
Maprs587780073
PheGenIrs587780073
hapmaprs587780073
1000 genomesrs587780073
hgdprs587780073
ensemblrs587780073
gopubmedrs587780073
geneviewrs587780073
scholarrs587780073
googlers587780073
pharmgkbrs587780073
gwascentralrs587780073
openSNPrs587780073
23andMers587780073
23andMe allrs587780073
SNP Nexus

SNPshotrs587780073
SNPdbers587780073
MSV3drs587780073
GWAS Ctlgrs587780073
Max Magnitude0
ClinVar
Risk rs587780073(G;G)
Alt rs587780073(G;G)
Reference rs587780073(A;A)
Significance Pathogenic
Disease not provided Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not provided Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577580T>C
CLNSRC
CLNACC RCV000115732.2, RCV000200601.1,