Variant (rsID / SNP)

rs1800466

rs1800466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAOA. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MAOAConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_000240.4(MAOA):c.1559A>G (p.Lys520Arg)
Allele change: Missense_K387R

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.