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rs876659802

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659802(C;T)
Make rs876659802(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7673787
GeneTP53
is asnp
is mentioned by
dbSNPrs876659802
ebirs876659802
HLIrs876659802
Exacrs876659802
Varsomers876659802
Maprs876659802
PheGenIrs876659802
hapmaprs876659802
1000 genomesrs876659802
hgdprs876659802
ensemblrs876659802
gopubmedrs876659802
geneviewrs876659802
scholarrs876659802
googlers876659802
pharmgkbrs876659802
gwascentralrs876659802
openSNPrs876659802
23andMers876659802
23andMe allrs876659802
SNP Nexus

SNPshotrs876659802
SNPdbers876659802
MSV3drs876659802
GWAS Ctlgrs876659802
Max Magnitude0
ClinVar
Risk rs876659802(T;T)
Alt rs876659802(T;T)
Reference rs876659802(C;C)
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.7577105G>A
CLNSRC
CLNACC RCV000214784.1,