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rs876658483

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658483(A;A)
Make rs876658483(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676211
GeneTP53
is asnp
is mentioned by
dbSNPrs876658483
ebirs876658483
HLIrs876658483
Exacrs876658483
Varsomers876658483
Maprs876658483
PheGenIrs876658483
hapmaprs876658483
1000 genomesrs876658483
hgdprs876658483
ensemblrs876658483
gopubmedrs876658483
geneviewrs876658483
scholarrs876658483
googlers876658483
pharmgkbrs876658483
gwascentralrs876658483
openSNPrs876658483
23andMers876658483
23andMe allrs876658483
SNP Nexus

SNPshotrs876658483
SNPdbers876658483
MSV3drs876658483
GWAS Ctlgrs876658483
Max Magnitude0
ClinVar
Risk rs876658483(A;A)
Alt rs876658483(A;A)
Reference rs876658483(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7579529C>T
CLNSRC
CLNACC RCV000222677.1,