Variant (rsID / SNP)

rs773658957

rs773658957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRDN. Location: chromosome 6, position 123,837,326. Clinical significance in the table: Likely benign.

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Reference-table entries

TRDNLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:123837326
Cytoband: 6q22.31
HGVS: NM_006073.4(TRDN):c.510A>G (p.Gly170=)
Allele change: Synonymous_G170G

Associated conditions / phenotypes

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.