List of variants in gene MAOA reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000240.4(MAOA):c.891G>T (p.Arg297=)	rs6323	0.71997
NM_000240.4(MAOA):c.1410T>C (p.Asp470=)	rs1137070	0.65298
NM_000240.4(MAOA):c.385A>C (p.Arg129=)	rs1800464	0.17743
NM_000240.4(MAOA):c.825G>A (p.Pro275=)	rs138703731	0.00238
NM_000240.4(MAOA):c.515G>A (p.Arg172Gln)	rs58524323	0.00220
NM_000240.4(MAOA):c.1559A>G (p.Lys520Arg)	rs1800466	0.00022
NM_000240.4(MAOA):c.412-6C>G	rs369122751	0.00011
NM_000240.4(MAOA):c.1498G>A (p.Gly500Ser)	rs1028101657	0.00002
NM_000240.4(MAOA):c.330C>T (p.Gly110=)	rs748344922	0.00002
NM_000240.4(MAOA):c.1079G>A (p.Arg360Gln)	rs755359800	0.00001
NM_000240.4(MAOA):c.1447_1448delinsAA (p.Ala483Lys)	rs1555951370
NM_000240.4(MAOA):c.555G>C (p.Glu185Asp)	rs2147101580

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.