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rs878854073

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854073(G;T)
Make rs878854073(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674291
GeneTP53
is asnp
is mentioned by
dbSNPrs878854073
ebirs878854073
HLIrs878854073
Exacrs878854073
Varsomers878854073
Maprs878854073
PheGenIrs878854073
hapmaprs878854073
1000 genomesrs878854073
hgdprs878854073
ensemblrs878854073
gopubmedrs878854073
geneviewrs878854073
scholarrs878854073
googlers878854073
pharmgkbrs878854073
gwascentralrs878854073
openSNPrs878854073
23andMers878854073
23andMe allrs878854073
SNP Nexus

SNPshotrs878854073
SNPdbers878854073
MSV3drs878854073
GWAS Ctlgrs878854073
Max Magnitude0
ClinVar
Risk rs878854073(T;T)
Alt rs878854073(T;T)
Reference rs878854073(G;G)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7577609C>A
CLNSRC
CLNACC RCV000228996.1,