Variant (rsID / SNP)

rs201545032

rs201545032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,695,832. 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: 7:91695832
Cytoband: 7q21.2
HGVS: NM_005751.5(AKAP9):c.6302A>G (p.Gln2101Arg)
Allele change: Missense_Q2101P

Associated conditions / phenotypes

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.