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

rs587783062

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783062(-;-)
Make rs587783062(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676102
GeneTP53
is asnp
is mentioned by
dbSNPrs587783062
ebirs587783062
HLIrs587783062
Exacrs587783062
Varsomers587783062
Maprs587783062
PheGenIrs587783062
hapmaprs587783062
1000 genomesrs587783062
hgdprs587783062
ensemblrs587783062
gopubmedrs587783062
geneviewrs587783062
scholarrs587783062
googlers587783062
pharmgkbrs587783062
gwascentralrs587783062
openSNPrs587783062
23andMers587783062
23andMe allrs587783062
SNP Nexus

SNPshotrs587783062
SNPdbers587783062
MSV3drs587783062
GWAS Ctlgrs587783062
Max Magnitude0
ClinVar
Risk rs587783062(;)
Alt rs587783062(;)
Reference rs587783062(C;C)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome 1
Reversed 1
HGVS NC_000017.10:g.7579420delG
CLNSRC
CLNACC RCV000144663.1,