Variant (rsID / SNP)

rs1063582

rs1063582 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXL2. Location: chromosome 8, position 23,167,353. The table records no clinical significance for this variant.

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Reference-table entries

LOXL2Not classified

Variant type: missense_variant
Chromosome / position: 8:23167353
HGVS: NM_002318.3,c.1708A>C,p.Met570Leu
Allele change: Missense_M570L

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.