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rs587781433

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781433(A;G)
Make rs587781433(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674197
GeneTP53
is asnp
is mentioned by
dbSNPrs587781433
ebirs587781433
HLIrs587781433
Exacrs587781433
Varsomers587781433
Maprs587781433
PheGenIrs587781433
hapmaprs587781433
1000 genomesrs587781433
hgdprs587781433
ensemblrs587781433
gopubmedrs587781433
geneviewrs587781433
scholarrs587781433
googlers587781433
pharmgkbrs587781433
gwascentralrs587781433
openSNPrs587781433
23andMers587781433
23andMe allrs587781433
SNP Nexus

SNPshotrs587781433
SNPdbers587781433
MSV3drs587781433
GWAS Ctlgrs587781433
Max Magnitude0
ClinVar
Risk rs587781433(G;G)
Alt rs587781433(G;G)
Reference rs587781433(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1
Reversed 1
HGVS NC_000017.10:g.7577515T>C
CLNSRC
CLNACC RCV000129326.2, RCV000172827.1,