Variant (rsID / SNP)
rs818817
rs818817 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A14. Location: chromosome 3, position 38,350,543. The table records no clinical significance for this variant.
Reference-table entries
SLC22A14Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:38350543
- HGVS
- NM_001320033.2,c.874A>G,p.Ser292Gly
- Allele change
- Missense_S292G
Associated conditions / phenotypes
Brugada Syndrome 1|Long Qt Syndrome 3|Brugada Syndrome|Ventricular Fibrillation, Paroxysmal Familial, 1|Progressive Familial Heart Block, Type Ia|Long Qt Syndrome|Sick Sinus Syndrome 1|Long Qt Syndrome 1|Cardiomyopathy, Dilated, 1e|Familial Long Qt Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.