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rs587780074

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780074(G;G)
Make rs587780074(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674226
GeneTP53
is asnp
is mentioned by
dbSNPrs587780074
ebirs587780074
HLIrs587780074
Exacrs587780074
Varsomers587780074
Maprs587780074
PheGenIrs587780074
hapmaprs587780074
1000 genomesrs587780074
hgdprs587780074
ensemblrs587780074
gopubmedrs587780074
geneviewrs587780074
scholarrs587780074
googlers587780074
pharmgkbrs587780074
gwascentralrs587780074
openSNPrs587780074
23andMers587780074
23andMe allrs587780074
SNP Nexus

SNPshotrs587780074
SNPdbers587780074
MSV3drs587780074
GWAS Ctlgrs587780074
Max Magnitude0
ClinVar
Risk rs587780074(G;G)
Alt rs587780074(G;G)
Reference rs587780074(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7577544A>C
CLNSRC
CLNACC RCV000115734.2,