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

rs587782160

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782160(A;T)
Make rs587782160(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675221
GeneTP53
is asnp
is mentioned by
dbSNPrs587782160
ebirs587782160
HLIrs587782160
Exacrs587782160
Varsomers587782160
Maprs587782160
PheGenIrs587782160
hapmaprs587782160
1000 genomesrs587782160
hgdprs587782160
ensemblrs587782160
gopubmedrs587782160
geneviewrs587782160
scholarrs587782160
googlers587782160
pharmgkbrs587782160
gwascentralrs587782160
openSNPrs587782160
23andMers587782160
23andMe allrs587782160
SNP Nexus

SNPshotrs587782160
SNPdbers587782160
MSV3drs587782160
GWAS Ctlgrs587782160
Max Magnitude0
ClinVar
Risk rs587782160(T;T)
Alt rs587782160(T;T)
Reference rs587782160(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578539T>A
CLNSRC
CLNACC RCV000130751.2,