Variant (rsID / SNP)

rs34210653

rs34210653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALOX15. Location: chromosome 17, position 4,535,314. Clinical significance in the table: Benign.

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Reference-table entries

ALOX15Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:4535314
Cytoband: 17p13.2
HGVS: NM_001140.5(ALOX15):c.1679C>T (p.Thr560Met)
Allele change: Missense_T560M

Associated conditions / phenotypes

Asthma, nasal polyps, and aspirin intolerance

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.