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rs876660726

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660726(-;-)
Make rs876660726(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7673718
GeneTP53
is asnp
is mentioned by
dbSNPrs876660726
ebirs876660726
HLIrs876660726
Exacrs876660726
Varsomers876660726
Maprs876660726
PheGenIrs876660726
hapmaprs876660726
1000 genomesrs876660726
hgdprs876660726
ensemblrs876660726
gopubmedrs876660726
geneviewrs876660726
scholarrs876660726
googlers876660726
pharmgkbrs876660726
gwascentralrs876660726
openSNPrs876660726
23andMers876660726
23andMe allrs876660726
SNP Nexus

SNPshotrs876660726
SNPdbers876660726
MSV3drs876660726
GWAS Ctlgrs876660726
Max Magnitude0
ClinVar
Risk rs876660726(;)
Alt rs876660726(;)
Reference rs876660726(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.7577036delG
CLNSRC
CLNACC RCV000219373.1,