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rs876658468

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658468(C;T)
Make rs876658468(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674954
GeneTP53
is asnp
is mentioned by
dbSNPrs876658468
ebirs876658468
HLIrs876658468
Exacrs876658468
Varsomers876658468
Maprs876658468
PheGenIrs876658468
hapmaprs876658468
1000 genomesrs876658468
hgdprs876658468
ensemblrs876658468
gopubmedrs876658468
geneviewrs876658468
scholarrs876658468
googlers876658468
pharmgkbrs876658468
gwascentralrs876658468
openSNPrs876658468
23andMers876658468
23andMe allrs876658468
SNP Nexus

SNPshotrs876658468
SNPdbers876658468
MSV3drs876658468
GWAS Ctlgrs876658468
Max Magnitude0
ClinVar
Risk rs876658468(T;T)
Alt rs876658468(T;T)
Reference rs876658468(C;C)
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.7578272G>A
CLNSRC
CLNACC RCV000221478.1,