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rs876658627

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658627(-;-)
Make rs876658627(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676543
GeneTP53
is asnp
is mentioned by
dbSNPrs876658627
ebirs876658627
HLIrs876658627
Exacrs876658627
Varsomers876658627
Maprs876658627
PheGenIrs876658627
hapmaprs876658627
1000 genomesrs876658627
hgdprs876658627
ensemblrs876658627
gopubmedrs876658627
geneviewrs876658627
scholarrs876658627
googlers876658627
pharmgkbrs876658627
gwascentralrs876658627
openSNPrs876658627
23andMers876658627
23andMe allrs876658627
SNP Nexus

SNPshotrs876658627
SNPdbers876658627
MSV3drs876658627
GWAS Ctlgrs876658627
Max Magnitude0
ClinVar
Risk rs876658627(;)
Alt rs876658627(;)
Reference rs876658627(A;A)
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.7579861delT
CLNSRC
CLNACC RCV000213243.1,