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rs863224451

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224451(A;A)
Make rs863224451(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7673796
GeneTP53
is asnp
is mentioned by
dbSNPrs863224451
ebirs863224451
HLIrs863224451
Exacrs863224451
Varsomers863224451
Maprs863224451
PheGenIrs863224451
hapmaprs863224451
1000 genomesrs863224451
hgdprs863224451
ensemblrs863224451
gopubmedrs863224451
geneviewrs863224451
scholarrs863224451
googlers863224451
pharmgkbrs863224451
gwascentralrs863224451
openSNPrs863224451
23andMers863224451
23andMe allrs863224451
SNP Nexus

SNPshotrs863224451
SNPdbers863224451
MSV3drs863224451
GWAS Ctlgrs863224451
Max Magnitude0
ClinVar
Risk rs863224451(A;A)
Alt rs863224451(A;A)
Reference rs863224451(G;G)
Significance Pathogenic
Disease Li-Fraumeni syndrome not provided
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome not provided
Reversed 1
HGVS NC_000017.10:g.7577114C>T
CLNSRC
CLNACC RCV000197359.1, RCV000235315.1,