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rs876659215

From SNPedia

Orientationminus
Geno Mag Summary
(CCGCCCGGCACCC;CCGCCCGGCACCC) 0 common in clinvar
Make rs876659215(-;-)
Make rs876659215(-;CCGCCCGGCACCC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7675146
GeneTP53
is asnp
is mentioned by
dbSNPrs876659215
ebirs876659215
HLIrs876659215
Exacrs876659215
Varsomers876659215
Maprs876659215
PheGenIrs876659215
hapmaprs876659215
1000 genomesrs876659215
hgdprs876659215
ensemblrs876659215
gopubmedrs876659215
geneviewrs876659215
scholarrs876659215
googlers876659215
pharmgkbrs876659215
gwascentralrs876659215
openSNPrs876659215
23andMers876659215
23andMe allrs876659215
SNP Nexus

SNPshotrs876659215
SNPdbers876659215
MSV3drs876659215
GWAS Ctlgrs876659215
Max Magnitude0
ClinVar
Risk rs876659215(;)
Alt rs876659215(;)
Reference rs876659215(CCGCCCGGCACCC;CCGCCCGGCACCC)
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.7578464_7578476delGGGTGCCGGGCGG
CLNSRC
CLNACC RCV000220919.1,