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rs55832599

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs55832599(A;A)
Make rs55832599(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position7673821
GeneTP53
is asnp
is mentioned by
dbSNPrs55832599
ebirs55832599
HLIrs55832599
Exacrs55832599
Varsomers55832599
Maprs55832599
PheGenIrs55832599
hapmaprs55832599
1000 genomesrs55832599
hgdprs55832599
ensemblrs55832599
gopubmedrs55832599
geneviewrs55832599
scholarrs55832599
googlers55832599
pharmgkbrs55832599
gwascentralrs55832599
openSNPrs55832599
23andMers55832599
23andMe allrs55832599
SNP Nexus

SNPshotrs55832599
SNPdbers55832599
MSV3drs55832599
GWAS Ctlgrs55832599
Max Magnitude0
ClinVar
Risk rs55832599(A;A)
Alt rs55832599(A;A)
Reference rs55832599(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.7577139G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000130398.2,