Variant (rsID / SNP)

rs184184931

rs184184931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,660,839. Clinical significance in the table: Likely benign.

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Reference-table entries

AKAP9Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:91660839
Cytoband: 7q21.2
HGVS: NM_005751.5(AKAP9):c.4259T>G (p.Phe1420Cys)
Allele change: Missense_F1420C

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.