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rs876659384

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659384(G;T)
Make rs876659384(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7673552
GeneTP53
is asnp
is mentioned by
dbSNPrs876659384
ebirs876659384
HLIrs876659384
Exacrs876659384
Varsomers876659384
Maprs876659384
PheGenIrs876659384
hapmaprs876659384
1000 genomesrs876659384
hgdprs876659384
ensemblrs876659384
gopubmedrs876659384
geneviewrs876659384
scholarrs876659384
googlers876659384
pharmgkbrs876659384
gwascentralrs876659384
openSNPrs876659384
23andMers876659384
23andMe allrs876659384
SNP Nexus

SNPshotrs876659384
SNPdbers876659384
MSV3drs876659384
GWAS Ctlgrs876659384
Max Magnitude0
ClinVar
Risk rs876659384(T;T)
Alt rs876659384(T;T)
Reference rs876659384(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.7576870C>A
CLNSRC
CLNACC RCV000218971.1,