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rs878854071

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854071(-;-)
Make rs878854071(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674869
GeneTP53
is asnp
is mentioned by
dbSNPrs878854071
ebirs878854071
HLIrs878854071
Exacrs878854071
Varsomers878854071
Maprs878854071
PheGenIrs878854071
hapmaprs878854071
1000 genomesrs878854071
hgdprs878854071
ensemblrs878854071
gopubmedrs878854071
geneviewrs878854071
scholarrs878854071
googlers878854071
pharmgkbrs878854071
gwascentralrs878854071
openSNPrs878854071
23andMers878854071
23andMe allrs878854071
SNP Nexus

SNPshotrs878854071
SNPdbers878854071
MSV3drs878854071
GWAS Ctlgrs878854071
Max Magnitude0
ClinVar
Risk rs878854071(;)
Alt rs878854071(;)
Reference rs878854071(A;A)
Significance Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7578187delT
CLNSRC
CLNACC RCV000234225.1,