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rs730882018

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882018(-;-)
Make rs730882018(-;C)
Make rs730882018(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7676152
GeneTP53
is asnp
is mentioned by
dbSNPrs730882018
ebirs730882018
HLIrs730882018
Exacrs730882018
Varsomers730882018
Maprs730882018
PheGenIrs730882018
hapmaprs730882018
1000 genomesrs730882018
hgdprs730882018
ensemblrs730882018
gopubmedrs730882018
geneviewrs730882018
scholarrs730882018
googlers730882018
pharmgkbrs730882018
gwascentralrs730882018
openSNPrs730882018
23andMers730882018
23andMe allrs730882018
SNP Nexus

SNPshotrs730882018
SNPdbers730882018
MSV3drs730882018
GWAS Ctlgrs730882018
Max Magnitude0
ClinVar
Risk rs730882018(C;C)
Alt rs730882018(C;C)
Reference rs730882018(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7579471dupG
CLNSRC
CLNACC RCV000161059.1, RCV000217506.1,