Variant (rsID / SNP)

rs17737379

rs17737379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRDN. Location: chromosome 6, position 123,696,766. Clinical significance in the table: Benign.

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Reference-table entries

TRDNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:123696766
Cytoband: 6q22.31
HGVS: NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu)
Allele change: Missense_D419E

Associated conditions / phenotypes

Cardiovascular phenotype|Catecholaminergic polymorphic ventricular tachycardia

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.