Variant (rsID / SNP)

rs150579291

rs150579291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,722,498. Clinical significance in the table: Uncertain significance.

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Reference-table entries

AKAP9Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:91722498
Cytoband: 7q21.2
HGVS: NM_005751.5(AKAP9):c.9446A>G (p.Glu3149Gly)
Allele change: Missense_E3141G

Associated conditions / phenotypes

Cardiovascular phenotype|Long QT 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.