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rs876659076

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659076(G;G)
Make rs876659076(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674179
GeneTP53
is asnp
is mentioned by
dbSNPrs876659076
ebirs876659076
HLIrs876659076
Exacrs876659076
Varsomers876659076
Maprs876659076
PheGenIrs876659076
hapmaprs876659076
1000 genomesrs876659076
hgdprs876659076
ensemblrs876659076
gopubmedrs876659076
geneviewrs876659076
scholarrs876659076
googlers876659076
pharmgkbrs876659076
gwascentralrs876659076
openSNPrs876659076
23andMers876659076
23andMe allrs876659076
SNP Nexus

SNPshotrs876659076
SNPdbers876659076
MSV3drs876659076
GWAS Ctlgrs876659076
Max Magnitude0
ClinVar
Risk rs876659076(G;G)
Alt rs876659076(G;G)
Reference rs876659076(T;T)
Significance Probable-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.7577497A>C
CLNSRC
CLNACC RCV000217728.1,