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rs863224499

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224499(A;A)
Make rs863224499(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7674858
GeneTP53
is asnp
is mentioned by
dbSNPrs863224499
ebirs863224499
HLIrs863224499
Exacrs863224499
Varsomers863224499
Maprs863224499
PheGenIrs863224499
hapmaprs863224499
1000 genomesrs863224499
hgdprs863224499
ensemblrs863224499
gopubmedrs863224499
geneviewrs863224499
scholarrs863224499
googlers863224499
pharmgkbrs863224499
gwascentralrs863224499
openSNPrs863224499
23andMers863224499
23andMe allrs863224499
SNP Nexus

SNPshotrs863224499
SNPdbers863224499
MSV3drs863224499
GWAS Ctlgrs863224499
Max Magnitude0
ClinVar
Risk rs863224499(A;A)
Alt rs863224499(A;A)
Reference rs863224499(G;G)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578176C>T
CLNSRC
CLNACC RCV000200333.2,