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rs587782490

From SNPedia

Orientationminus
Geno Mag Summary
(CGTCTGGGCTTC;CGTCTGGGCTTC) 0 common in clinvar
Make rs587782490(-;-)
Make rs587782490(-;CGTCTGGGCTTC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676030
GeneTP53
is asnp
is mentioned by
dbSNPrs587782490
ebirs587782490
HLIrs587782490
Exacrs587782490
Varsomers587782490
Maprs587782490
PheGenIrs587782490
hapmaprs587782490
1000 genomesrs587782490
hgdprs587782490
ensemblrs587782490
gopubmedrs587782490
geneviewrs587782490
scholarrs587782490
googlers587782490
pharmgkbrs587782490
gwascentralrs587782490
openSNPrs587782490
23andMers587782490
23andMe allrs587782490
SNP Nexus

SNPshotrs587782490
SNPdbers587782490
MSV3drs587782490
GWAS Ctlgrs587782490
Max Magnitude0
ClinVar
Risk rs587782490(;)
Alt rs587782490(;)
Reference rs587782490(CGTCTGGGCTTC;CGTCTGGGCTTC)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579348_7579359delGAAGCCCAGACG
CLNSRC
CLNACC RCV000131618.2,