List of variants in gene MAK reported as likely benign for perceptual disorders

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

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001242957.3(MAK):c.1715T>C (p.Ile572Thr)	rs79544660	0.00488
NM_001242957.3(MAK):c.1151A>G (p.Asn384Ser)	rs55773478	0.00019
NM_001242957.3(MAK):c.1119G>A (p.Pro373=)	rs1011259942	0.00003
NM_001242957.3(MAK):c.1062C>T (p.Ser354=)	rs199694073	0.00001
NM_001242957.3(MAK):c.1315C>T (p.Arg439Trp)	rs764870230	0.00001
NM_001242957.3(MAK):c.968C>G (p.Pro323Arg)	rs200641218	0.00001
NM_001242957.3(MAK):c.1353G>T (p.Ser451=)
NM_001242957.3(MAK):c.369T>C (p.His123=)

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