Variant (rsID / SNP)

rs586339

rs586339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDM4A. Location: chromosome 1, position 44,137,257. The table records no clinical significance for this variant.

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Reference-table entries

KDM4ANot classified

Variant type: missense_variant
Chromosome / position: 1:44137257
HGVS: NM_014663.3,c.1445C>A,p.Ala482Glu
Allele change: Missense_A482E

Associated conditions / phenotypes

Lung Cancer

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.