ClinVar Miner

List of variants in gene MAOA studied for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_000240.3(MAOA):c.133C>T (p.Arg45Trp) rs796065312
NM_000240.3(MAOA):c.1545G>T (p.Gly515=) rs1223537199
NM_000240.3(MAOA):c.168+11_168+15del rs375984321
NM_000240.3(MAOA):c.260A>G (p.Glu87Gly) rs747229681
NM_000240.3(MAOA):c.3G>A (p.Met1Ile) rs1601921232
NM_000240.3(MAOA):c.402G>A (p.Met134Ile) rs771740634
NM_000240.3(MAOA):c.515G>A (p.Arg172Gln) rs58524323
NM_000240.3(MAOA):c.702C>T (p.Leu234=) rs370853887
NM_000240.3(MAOA):c.730G>A (p.Val244Ile) rs1135401773
NM_000240.3(MAOA):c.74-6C>T rs1196492976
NM_000240.3(MAOA):c.749_750insT (p.Ser251fs) rs796065311
NM_000240.3(MAOA):c.797G>T (p.Cys266Phe) rs587777457
NM_000240.3(MAOA):c.816G>A (p.Ala272=) rs751223564
NM_000240.3(MAOA):c.825G>A (p.Pro275=) rs138703731
NM_000240.3(MAOA):c.886C>T (p.Gln296Ter) rs72554632
NM_000240.3(MAOA):c.890G>A (p.Arg297Gln) rs780647851

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