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rs587780070

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780070(C;T)
Make rs587780070(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675077
GeneTP53
is asnp
is mentioned by
dbSNPrs587780070
ebirs587780070
HLIrs587780070
Exacrs587780070
Varsomers587780070
Maprs587780070
PheGenIrs587780070
hapmaprs587780070
1000 genomesrs587780070
hgdprs587780070
ensemblrs587780070
gopubmedrs587780070
geneviewrs587780070
scholarrs587780070
googlers587780070
pharmgkbrs587780070
gwascentralrs587780070
openSNPrs587780070
23andMers587780070
23andMe allrs587780070
SNP Nexus

SNPshotrs587780070
SNPdbers587780070
MSV3drs587780070
GWAS Ctlgrs587780070
Max Magnitude0
ClinVar
Risk rs587780070(T;T)
Alt rs587780070(T;T)
Reference rs587780070(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7578395G>A
CLNSRC
CLNACC RCV000115726.3,