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rs876658144

From SNPedia

Orientationminus
Geno Mag Summary
(CTATGAGCC;CTATGAGCC) 0 common in clinvar
Make rs876658144(-;-)
Make rs876658144(-;CTATGAGCC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674866
GeneTP53
is asnp
is mentioned by
dbSNPrs876658144
ebirs876658144
HLIrs876658144
Exacrs876658144
Varsomers876658144
Maprs876658144
PheGenIrs876658144
hapmaprs876658144
1000 genomesrs876658144
hgdprs876658144
ensemblrs876658144
gopubmedrs876658144
geneviewrs876658144
scholarrs876658144
googlers876658144
pharmgkbrs876658144
gwascentralrs876658144
openSNPrs876658144
23andMers876658144
23andMe allrs876658144
SNP Nexus

SNPshotrs876658144
SNPdbers876658144
MSV3drs876658144
GWAS Ctlgrs876658144
Max Magnitude0
ClinVar
Risk rs876658144(;)
Alt rs876658144(;)
Reference rs876658144(CTATGAGCC;CTATGAGCC)
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.7578184_7578192delGGCTCATAG
CLNSRC
CLNACC RCV000222764.1,