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rs730882006

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882006(C;C)
Make rs730882006(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674235
GeneTP53
is asnp
is mentioned by
dbSNPrs730882006
ebirs730882006
HLIrs730882006
Exacrs730882006
Varsomers730882006
Maprs730882006
PheGenIrs730882006
hapmaprs730882006
1000 genomesrs730882006
hgdprs730882006
ensemblrs730882006
gopubmedrs730882006
geneviewrs730882006
scholarrs730882006
googlers730882006
pharmgkbrs730882006
gwascentralrs730882006
openSNPrs730882006
23andMers730882006
23andMe allrs730882006
SNP Nexus

SNPshotrs730882006
SNPdbers730882006
MSV3drs730882006
GWAS Ctlgrs730882006
Max Magnitude0
ClinVar
Risk rs730882006(C;C)
Alt rs730882006(C;C)
Reference rs730882006(T;T)
Significance Probable-Pathogenic
Disease not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7577553A>G
CLNSRC
CLNACC RCV000161035.1, RCV000222280.1,