Variant (rsID / SNP)

rs79447697

rs79447697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSEN34. Location: chromosome 19, position 54,698,348. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TSEN34Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:54698348
Cytoband: 19q13.42
HGVS: NM_001077446.4(TSEN34):c.*1128G>T
Allele change: Silent

Associated conditions / phenotypes

Pontoneocerebellar hypoplasia

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.