Variant (rsID / SNP)

rs1059485

rs1059485 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPTIN9. Location: chromosome 17, position 75,494,746. Clinical significance in the table: Benign.

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Reference-table entries

SEPTIN9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:75494746
Cytoband: 17q25.3
HGVS: NM_001113491.2(SEPTIN9):c.*6A>G
Allele change: Silent

Associated conditions / phenotypes

Amyotrophic neuralgia

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.