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rs397516438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTCC;TTCC) 0 common in clinvar
Make rs397516438(AAGAACGT;AAGAACGT)
Make rs397516438(AAGAACGT;TTCC)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676398
GeneTP53
is asnp
is mentioned by
dbSNPrs397516438
ebirs397516438
HLIrs397516438
Exacrs397516438
Varsomers397516438
Maprs397516438
PheGenIrs397516438
hapmaprs397516438
1000 genomesrs397516438
hgdprs397516438
ensemblrs397516438
gopubmedrs397516438
geneviewrs397516438
scholarrs397516438
googlers397516438
pharmgkbrs397516438
gwascentralrs397516438
openSNPrs397516438
23andMers397516438
23andMe allrs397516438
SNP Nexus

SNPshotrs397516438
SNPdbers397516438
MSV3drs397516438
GWAS Ctlgrs397516438
Max Magnitude0
ClinVar
Risk rs397516438(AAGAACGT;AAGAACGT)
Alt rs397516438(AAGAACGT;AAGAACGT)
Reference rs397516438(TTCC;TTCC)
Significance Probable-Pathogenic
Disease Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579716_7579719delGGAAinsACGTTCTT
CLNSRC ClinVar
CLNACC RCV000036535.2,