Variant (rsID / SNP)

rs150016098

rs150016098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,674,405. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AKAP9Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:91674405
Cytoband: 7q21.2
HGVS: NM_005751.5(AKAP9):c.5246T>C (p.Ile1749Thr)
Allele change: Missense_I1749T

Associated conditions / phenotypes

Cardiovascular phenotype|Long QT syndrome 11|unspecified heart condition|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.