Variant (rsID / SNP)

rs148596612

rs148596612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRDN. Location: chromosome 6, position 123,837,328. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TRDNBenign

Clinical significance (as recorded): Benign
Variant type: Microsatellite
Chromosome / position: 6:123837328
Cytoband: 6q22.31
HGVS: NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1])

Associated conditions / phenotypes

Catecholaminergic polymorphic ventricular tachycardia|Cardiovascular phenotype|Catecholaminergic polymorphic ventricular tachycardia 5

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.