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rs193920817

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193920817(A;A)
Make rs193920817(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7675131
GeneTP53
is asnp
is mentioned by
dbSNPrs193920817
ebirs193920817
HLIrs193920817
Exacrs193920817
Varsomers193920817
Maprs193920817
PheGenIrs193920817
hapmaprs193920817
1000 genomesrs193920817
hgdprs193920817
ensemblrs193920817
gopubmedrs193920817
geneviewrs193920817
scholarrs193920817
googlers193920817
pharmgkbrs193920817
gwascentralrs193920817
openSNPrs193920817
23andMers193920817
23andMe allrs193920817
SNP Nexus

SNPshotrs193920817
SNPdbers193920817
MSV3drs193920817
GWAS Ctlgrs193920817
Max Magnitude0
ClinVar
Risk rs193920817(A;A)
Alt rs193920817(A;A)
Reference rs193920817(G;G)
Significance Probable-Pathogenic
Disease Malignant tumor of prostate not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Malignant tumor of prostate not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7578449C>T
CLNSRC
CLNACC RCV000149053.1, RCV000161027.1, RCV000214033.1,