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rs587780071

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780071(C;T)
Make rs587780071(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674951
GeneTP53
is asnp
is mentioned by
dbSNPrs587780071
ebirs587780071
HLIrs587780071
Exacrs587780071
Varsomers587780071
Maprs587780071
PheGenIrs587780071
hapmaprs587780071
1000 genomesrs587780071
hgdprs587780071
ensemblrs587780071
gopubmedrs587780071
geneviewrs587780071
scholarrs587780071
googlers587780071
pharmgkbrs587780071
gwascentralrs587780071
openSNPrs587780071
23andMers587780071
23andMe allrs587780071
SNP Nexus

SNPshotrs587780071
SNPdbers587780071
MSV3drs587780071
GWAS Ctlgrs587780071
Max Magnitude0
ClinVar
Risk rs587780071(T;T)
Alt rs587780071(T;T)
Reference rs587780071(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7578269G>A
CLNSRC
CLNACC RCV000115728.2,