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rs876658483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658483(A;A)
Make rs876658483(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676211
GeneTP53
is asnp
is mentioned by
dbSNPrs876658483
dbSNP (classic)rs876658483
ClinGenrs876658483
ebirs876658483
HLIrs876658483
Exacrs876658483
Gnomadrs876658483
Varsomers876658483
LitVarrs876658483
Maprs876658483
PheGenIrs876658483
Biobankrs876658483
1000 genomesrs876658483
hgdprs876658483
ensemblrs876658483
geneviewrs876658483
scholarrs876658483
googlers876658483
pharmgkbrs876658483
gwascentralrs876658483
openSNPrs876658483
23andMers876658483
SNPshotrs876658483
SNPdbers876658483
MSV3drs876658483
GWAS Ctlgrs876658483
Max Magnitude0
ClinVar
Risk rs876658483(A;A)
Alt rs876658483(A;A)
Reference Rs876658483(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.7579529C>T
CLNSRC
CLNACC RCV000222677.1,