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rs397516439

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516439(A;G)
Make rs397516439(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7673610
GeneTP53
is asnp
is mentioned by
dbSNPrs397516439
ebirs397516439
HLIrs397516439
Exacrs397516439
Varsomers397516439
Maprs397516439
PheGenIrs397516439
hapmaprs397516439
1000 genomesrs397516439
hgdprs397516439
ensemblrs397516439
gopubmedrs397516439
geneviewrs397516439
scholarrs397516439
googlers397516439
pharmgkbrs397516439
gwascentralrs397516439
openSNPrs397516439
23andMers397516439
23andMe allrs397516439
SNP Nexus

SNPshotrs397516439
SNPdbers397516439
MSV3drs397516439
GWAS Ctlgrs397516439
Max Magnitude0
ClinVar
Risk rs397516439(G;G)
Alt rs397516439(G;G)
Reference rs397516439(A;A)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7576928T>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000036537.2, RCV000132190.2,