Variant (rsID / SNP)

rs3825942

rs3825942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXL1. Location: chromosome 15, position 74,219,582. Clinical significance in the table: risk factor.

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Reference-table entries

LOXL1Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 15:74219582
Cytoband: 15q24.1
HGVS: NM_005576.4(LOXL1):c.458G>A (p.Gly153Asp)
Allele change: Silent

Associated conditions / phenotypes

Exfoliation syndrome, susceptibility to

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.