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rs587782393

From SNPedia

Orientationminus
Geno Mag Summary
(CACACCCCCGCCC;CACACCCCCGCCC) 0 common in clinvar
Make rs587782393(-;-)
Make rs587782393(-;CACACCCCCGCCC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675153
GeneTP53
is asnp
is mentioned by
dbSNPrs587782393
ebirs587782393
HLIrs587782393
Exacrs587782393
Varsomers587782393
Maprs587782393
PheGenIrs587782393
hapmaprs587782393
1000 genomesrs587782393
hgdprs587782393
ensemblrs587782393
gopubmedrs587782393
geneviewrs587782393
scholarrs587782393
googlers587782393
pharmgkbrs587782393
gwascentralrs587782393
openSNPrs587782393
23andMers587782393
23andMe allrs587782393
SNP Nexus

SNPshotrs587782393
SNPdbers587782393
MSV3drs587782393
GWAS Ctlgrs587782393
Max Magnitude0
ClinVar
Risk rs587782393(;)
Alt rs587782393(;)
Reference rs587782393(CACACCCCCGCCC;CACACCCCCGCCC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7578471_7578483delGGGCGGGGGTGTG
CLNSRC
CLNACC RCV000131407.2,