Variant (rsID / SNP)

rs1800449

rs1800449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOX. Location: chromosome 5, position 121,413,208. Clinical significance in the table: Benign.

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Reference-table entries

LOXBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:121413208
Cytoband: 5q23.1
HGVS: NM_002317.7(LOX):c.473G>A (p.Arg158Gln)
Allele change: Missense_R158Q

Associated conditions / phenotypes

LYSYL OXIDASE POLYMORPHISM

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.