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rs876658982

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658982(A;A)
Make rs876658982(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7669691
GeneTP53
is asnp
is mentioned by
dbSNPrs876658982
ebirs876658982
HLIrs876658982
Exacrs876658982
Varsomers876658982
Maprs876658982
PheGenIrs876658982
hapmaprs876658982
1000 genomesrs876658982
hgdprs876658982
ensemblrs876658982
gopubmedrs876658982
geneviewrs876658982
scholarrs876658982
googlers876658982
pharmgkbrs876658982
gwascentralrs876658982
openSNPrs876658982
23andMers876658982
23andMe allrs876658982
SNP Nexus

SNPshotrs876658982
SNPdbers876658982
MSV3drs876658982
GWAS Ctlgrs876658982
Max Magnitude0
ClinVar
Risk rs876658982(A;A)
Alt rs876658982(A;A)
Reference rs876658982(G;G)
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.7573009C>T
CLNSRC
CLNACC RCV000222547.1,