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rs483352696

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483352696(A;G)
Make rs483352696(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673733
GeneTP53
is asnp
is mentioned by
dbSNPrs483352696
ebirs483352696
HLIrs483352696
Exacrs483352696
Varsomers483352696
Maprs483352696
PheGenIrs483352696
hapmaprs483352696
1000 genomesrs483352696
hgdprs483352696
ensemblrs483352696
gopubmedrs483352696
geneviewrs483352696
scholarrs483352696
googlers483352696
pharmgkbrs483352696
gwascentralrs483352696
openSNPrs483352696
23andMers483352696
23andMe allrs483352696
SNP Nexus

SNPshotrs483352696
SNPdbers483352696
MSV3drs483352696
GWAS Ctlgrs483352696
Max Magnitude0
ClinVar
Risk rs483352696(G;G)
Alt rs483352696(G;G)
Reference rs483352696(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7577051T>C
CLNSRC
CLNACC RCV000087174.2,