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rs730882015

From SNPedia

Orientationminus
Geno Mag Summary
(TTCC;TTCC) 0 common in clinvar
Make rs730882015(-;-)
Make rs730882015(-;TTCC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676072
GeneTP53
is asnp
is mentioned by
dbSNPrs730882015
ebirs730882015
HLIrs730882015
Exacrs730882015
Varsomers730882015
Maprs730882015
PheGenIrs730882015
hapmaprs730882015
1000 genomesrs730882015
hgdprs730882015
ensemblrs730882015
gopubmedrs730882015
geneviewrs730882015
scholarrs730882015
googlers730882015
pharmgkbrs730882015
gwascentralrs730882015
openSNPrs730882015
23andMers730882015
23andMe allrs730882015
SNP Nexus

SNPshotrs730882015
SNPdbers730882015
MSV3drs730882015
GWAS Ctlgrs730882015
Max Magnitude0
ClinVar
Risk rs730882015(;)
Alt rs730882015(;)
Reference rs730882015(TTCC;TTCC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579390_7579393delGGAA
CLNSRC
CLNACC RCV000161056.1,