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rs730882001

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882001(C;T)
Make rs730882001(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675119
GeneTP53
is asnp
is mentioned by
dbSNPrs730882001
ebirs730882001
HLIrs730882001
Exacrs730882001
Varsomers730882001
Maprs730882001
PheGenIrs730882001
hapmaprs730882001
1000 genomesrs730882001
hgdprs730882001
ensemblrs730882001
gopubmedrs730882001
geneviewrs730882001
scholarrs730882001
googlers730882001
pharmgkbrs730882001
gwascentralrs730882001
openSNPrs730882001
23andMers730882001
23andMe allrs730882001
SNP Nexus

SNPshotrs730882001
SNPdbers730882001
MSV3drs730882001
GWAS Ctlgrs730882001
Max Magnitude0
ClinVar
Risk rs730882001(T;T)
Alt rs730882001(T;T)
Reference rs730882001(C;C)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7578437G>A
CLNSRC
CLNACC RCV000161028.1, RCV000219202.1,