Variant (rsID / SNP)

rs138703731

rs138703731 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.825G>A (p.Pro275=)
Allele change: Synonymous_P142P

Associated conditions / phenotypes

Brunner syndrome|History of neurodevelopmental disorder

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.