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rs876660807

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660807(A;G)
Make rs876660807(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674248
GeneTP53
is asnp
is mentioned by
dbSNPrs876660807
ebirs876660807
HLIrs876660807
Exacrs876660807
Varsomers876660807
Maprs876660807
PheGenIrs876660807
hapmaprs876660807
1000 genomesrs876660807
hgdprs876660807
ensemblrs876660807
gopubmedrs876660807
geneviewrs876660807
scholarrs876660807
googlers876660807
pharmgkbrs876660807
gwascentralrs876660807
openSNPrs876660807
23andMers876660807
23andMe allrs876660807
SNP Nexus

SNPshotrs876660807
SNPdbers876660807
MSV3drs876660807
GWAS Ctlgrs876660807
Max Magnitude0
ClinVar
Risk rs876660807(G;G)
Alt rs876660807(G;G)
Reference rs876660807(A;A)
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.7577566T>C
CLNSRC
CLNACC RCV000223044.1,