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rs730882016

From SNPedia

Orientationminus
Geno Mag Summary
(TGTACCAC;TGTACCAC) 0 common in clinvar
Make rs730882016(-;-)
Make rs730882016(-;TGTACCAC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674271
GeneTP53
is asnp
is mentioned by
dbSNPrs730882016
ebirs730882016
HLIrs730882016
Exacrs730882016
Varsomers730882016
Maprs730882016
PheGenIrs730882016
hapmaprs730882016
1000 genomesrs730882016
hgdprs730882016
ensemblrs730882016
gopubmedrs730882016
geneviewrs730882016
scholarrs730882016
googlers730882016
pharmgkbrs730882016
gwascentralrs730882016
openSNPrs730882016
23andMers730882016
23andMe allrs730882016
SNP Nexus

SNPshotrs730882016
SNPdbers730882016
MSV3drs730882016
GWAS Ctlgrs730882016
Max Magnitude0
ClinVar
Risk rs730882016(;)
Alt rs730882016(;)
Reference rs730882016(TGTACCAC;TGTACCAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577589_7577596delGTGGTACA
CLNSRC
CLNACC RCV000161057.1,