Variant (rsID / SNP)

rs34875865

rs34875865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP63. Location: chromosome 3, position 189,455,681. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TP63Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:189455681
Cytoband: 3q28
HGVS: NM_003722.5(TP63):c.191+24T>C
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.