List of variants in gene MAOA reported as pathogenic for X-linked disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NC_000023.10:g.(?_43515570)_(43603780_?)del
NM_000240.4(MAOA):c.1214del (p.Gly405fs)	rs2147107556
NM_000240.4(MAOA):c.133C>T (p.Arg45Trp)	rs796065312
NM_000240.4(MAOA):c.749_750insT (p.Ser251fs)	rs796065311
NM_000240.4(MAOA):c.797G>T (p.Cys266Phe)	rs587777457
NM_000240.4(MAOA):c.886C>T (p.Gln296Ter)	rs72554632

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