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rs730882027

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882027(G;G)
Make rs730882027(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7674211
GeneTP53
is asnp
is mentioned by
dbSNPrs730882027
ebirs730882027
HLIrs730882027
Exacrs730882027
Varsomers730882027
Maprs730882027
PheGenIrs730882027
hapmaprs730882027
1000 genomesrs730882027
hgdprs730882027
ensemblrs730882027
gopubmedrs730882027
geneviewrs730882027
scholarrs730882027
googlers730882027
pharmgkbrs730882027
gwascentralrs730882027
openSNPrs730882027
23andMers730882027
23andMe allrs730882027
SNP Nexus

SNPshotrs730882027
SNPdbers730882027
MSV3drs730882027
GWAS Ctlgrs730882027
Max Magnitude0
ClinVar
Risk rs730882027(G;G)
Alt rs730882027(G;G)
Reference rs730882027(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7577529A>C
CLNSRC
CLNACC RCV000161070.2,