Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224500

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224500(G;T)
Make rs863224500(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7673555
GeneTP53
is asnp
is mentioned by
dbSNPrs863224500
ebirs863224500
HLIrs863224500
Exacrs863224500
Varsomers863224500
Maprs863224500
PheGenIrs863224500
hapmaprs863224500
1000 genomesrs863224500
hgdprs863224500
ensemblrs863224500
gopubmedrs863224500
geneviewrs863224500
scholarrs863224500
googlers863224500
pharmgkbrs863224500
gwascentralrs863224500
openSNPrs863224500
23andMers863224500
23andMe allrs863224500
SNP Nexus

SNPshotrs863224500
SNPdbers863224500
MSV3drs863224500
GWAS Ctlgrs863224500
Max Magnitude0
ClinVar
Risk rs863224500(T;T)
Alt rs863224500(T;T)
Reference rs863224500(G;G)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7576873C>A
CLNSRC
CLNACC RCV000195434.2,