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rs587781288

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781288(A;A)
Make rs587781288(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675190
GeneTP53
is asnp
is mentioned by
dbSNPrs587781288
ebirs587781288
HLIrs587781288
Exacrs587781288
Varsomers587781288
Maprs587781288
PheGenIrs587781288
hapmaprs587781288
1000 genomesrs587781288
hgdprs587781288
ensemblrs587781288
gopubmedrs587781288
geneviewrs587781288
scholarrs587781288
googlers587781288
pharmgkbrs587781288
gwascentralrs587781288
openSNPrs587781288
23andMers587781288
23andMe allrs587781288
SNP Nexus

SNPshotrs587781288
SNPdbers587781288
MSV3drs587781288
GWAS Ctlgrs587781288
Max Magnitude0
ClinVar
Risk rs587781288(A;A)
Alt rs587781288(A;A)
Reference rs587781288(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578508C>T
CLNSRC
CLNACC RCV000128975.2,