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

rs587780067

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587780067(-;-)
Make rs587780067(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676003
GeneTP53
is asnp
is mentioned by
dbSNPrs587780067
ebirs587780067
HLIrs587780067
Exacrs587780067
Varsomers587780067
Maprs587780067
PheGenIrs587780067
hapmaprs587780067
1000 genomesrs587780067
hgdprs587780067
ensemblrs587780067
gopubmedrs587780067
geneviewrs587780067
scholarrs587780067
googlers587780067
pharmgkbrs587780067
gwascentralrs587780067
openSNPrs587780067
23andMers587780067
23andMe allrs587780067
SNP Nexus

SNPshotrs587780067
SNPdbers587780067
MSV3drs587780067
GWAS Ctlgrs587780067
Max Magnitude0
ClinVar
Risk rs587780067(;)
Alt rs587780067(;)
Reference rs587780067(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7579321_7579322delCA
CLNSRC
CLNACC RCV000115720.3,