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rs730882025

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882025(A;A)
Make rs730882025(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674885
GeneTP53
is asnp
is mentioned by
dbSNPrs730882025
ebirs730882025
HLIrs730882025
Exacrs730882025
Varsomers730882025
Maprs730882025
PheGenIrs730882025
hapmaprs730882025
1000 genomesrs730882025
hgdprs730882025
ensemblrs730882025
gopubmedrs730882025
geneviewrs730882025
scholarrs730882025
googlers730882025
pharmgkbrs730882025
gwascentralrs730882025
openSNPrs730882025
23andMers730882025
23andMe allrs730882025
SNP Nexus

SNPshotrs730882025
SNPdbers730882025
MSV3drs730882025
GWAS Ctlgrs730882025
Max Magnitude0
ClinVar
Risk rs730882025(A;A)
Alt rs730882025(A;A)
Reference rs730882025(G;G)
Significance Probable-Pathogenic
Disease not provided Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not provided Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578203C>T
CLNSRC
CLNACC RCV000161067.2, RCV000168150.1,