Variant (rsID / SNP)

rs9840360

rs9840360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP63. Location: chromosome 3, position 189,590,825. Clinical significance in the table: Benign.

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Reference-table entries

TP63Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:189590825
Cytoband: 3q28
HGVS: NM_003722.5(TP63):c.1349+41G>A
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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