Have questions? Visit https://www.reddit.com/r/SNPedia

rs786201059

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201059(A;A)
Make rs786201059(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7673764
GeneTP53
is asnp
is mentioned by
dbSNPrs786201059
ebirs786201059
HLIrs786201059
Exacrs786201059
Varsomers786201059
Maprs786201059
PheGenIrs786201059
hapmaprs786201059
1000 genomesrs786201059
hgdprs786201059
ensemblrs786201059
gopubmedrs786201059
geneviewrs786201059
scholarrs786201059
googlers786201059
pharmgkbrs786201059
gwascentralrs786201059
openSNPrs786201059
23andMers786201059
23andMe allrs786201059
SNP Nexus

SNPshotrs786201059
SNPdbers786201059
MSV3drs786201059
GWAS Ctlgrs786201059
Max Magnitude0
ClinVar
Risk rs786201059(A;A)
Alt rs786201059(A;A)
Reference rs786201059(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577082C>T
CLNSRC
CLNACC RCV000162466.1,