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Variant (rsID / SNP)

rs78378222

TP53

rs78378222 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,571,752. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TP53Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:7571752
Cytoband
17p13.1
HGVS
NM_000546.6(TP53):c.*1175A>C
Allele change
Silent

Associated conditions / phenotypes

Basal cell carcinoma, susceptibility to, 7|Li-Fraumeni syndrome 1|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.