Variant (rsID / SNP)

rs34587622

rs34587622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPTIN9. Location: chromosome 17, position 75,398,498. 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: 17:75398498
Cytoband: 17q25.3
HGVS: NM_001113491.2(SEPTIN9):c.434C>T (p.Pro145Leu)
Allele change: Missense_P126L

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.