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rs587781504

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781504(A;A)
Make rs587781504(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7676055
GeneTP53
is asnp
is mentioned by
dbSNPrs587781504
ebirs587781504
HLIrs587781504
Exacrs587781504
Varsomers587781504
Maprs587781504
PheGenIrs587781504
hapmaprs587781504
1000 genomesrs587781504
hgdprs587781504
ensemblrs587781504
gopubmedrs587781504
geneviewrs587781504
scholarrs587781504
googlers587781504
pharmgkbrs587781504
gwascentralrs587781504
openSNPrs587781504
23andMers587781504
23andMe allrs587781504
SNP Nexus

SNPshotrs587781504
SNPdbers587781504
MSV3drs587781504
GWAS Ctlgrs587781504
Max Magnitude0
ClinVar
Risk rs587781504(A;A)
Alt rs587781504(A;A)
Reference rs587781504(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome not provided Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579373C>T
CLNSRC
CLNACC RCV000129479.5, RCV000201000.1, RCV000228756.1,