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

rs587776768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAA;AAA) 0 common in clinvar
(TT;TT) 0 common in clinvar
Make rs587776768(-;-)
Make rs587776768(-;TT)
ReferenceGRCh38 38.1/142
Chromosome17
Position7674903
GeneTP53
is asnp
is mentioned by
dbSNPrs587776768
ebirs587776768
HLIrs587776768
Exacrs587776768
Varsomers587776768
Maprs587776768
PheGenIrs587776768
hapmaprs587776768
1000 genomesrs587776768
hgdprs587776768
ensemblrs587776768
gopubmedrs587776768
geneviewrs587776768
scholarrs587776768
googlers587776768
pharmgkbrs587776768
gwascentralrs587776768
openSNPrs587776768
23andMers587776768
23andMe allrs587776768
SNP Nexus

SNPshotrs587776768
SNPdbers587776768
MSV3drs587776768
GWAS Ctlgrs587776768
Max Magnitude0
ClinVar
Risk rs587776768(TTA,A;TTA,A)
Alt rs587776768(TTA,A;TTA,A)
Reference rs587776768(AAA;AAA)
Significance Pathogenic
Disease Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome 1
Reversed 1
HGVS NC_000017.10:g.7578221_7578222delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000013156.22,