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rs587781589

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781589(C;C)
Make rs587781589(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674268
GeneTP53
is asnp
is mentioned by
dbSNPrs587781589
ebirs587781589
HLIrs587781589
Exacrs587781589
Varsomers587781589
Maprs587781589
PheGenIrs587781589
hapmaprs587781589
1000 genomesrs587781589
hgdprs587781589
ensemblrs587781589
gopubmedrs587781589
geneviewrs587781589
scholarrs587781589
googlers587781589
pharmgkbrs587781589
gwascentralrs587781589
openSNPrs587781589
23andMers587781589
23andMe allrs587781589
SNP Nexus

SNPshotrs587781589
SNPdbers587781589
MSV3drs587781589
GWAS Ctlgrs587781589
Max Magnitude0
ClinVar
Risk rs587781589(C;C)
Alt rs587781589(C;C)
Reference rs587781589(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577586A>G
CLNSRC
CLNACC RCV000129637.2,