Variant (rsID / SNP)

rs1983864

rs1983864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOXL4. Location: chromosome 10, position 100,017,453. The table records no clinical significance for this variant.

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Reference-table entries

LOXL4Not classified

Variant type: missense_variant
Chromosome / position: 10:100017453
HGVS: NM_032211.7,c.1214A>C,p.Asp405Ala
Allele change: Missense_D405A

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.