Variant (rsID / SNP)

rs1800464

rs1800464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAOA. Clinical significance in the table: Benign.

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Reference-table entries

MAOABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_000240.4(MAOA):c.385A>C (p.Arg129=)
Allele change: Silent

Associated conditions / phenotypes

History of neurodevelopmental disorder|Brunner syndrome

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.