Variant (rsID / SNP)

rs17058639

rs17058639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLMAP. Location: chromosome 3, position 57,882,601. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLMAPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:57882601
Cytoband: 3p14.3
HGVS: NM_001377540.1(SLMAP):c.1443C>T (p.Asp481=)
Allele change: Synonymous_D426D

Associated conditions / phenotypes

Brugada syndrome

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.