List of variants in gene MANBA reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005908.4(MANBA):c.2015-28G>A	rs4547797	0.55331
NM_005908.4(MANBA):c.2368T>C (p.Leu790=)	rs2272697	0.55313
NM_005908.4(MANBA):c.757G>A (p.Val253Ile)	rs227368	0.39095
NM_005908.4(MANBA):c.315G>A (p.Thr105=)	rs6857760	0.10011
NM_005908.4(MANBA):c.831A>G (p.Leu277=)	rs17033168	0.04331
NM_005908.4(MANBA):c.1482G>T (p.Leu494=)	rs74718667	0.02371
NM_005908.4(MANBA):c.2482G>A (p.Val828Ile)	rs75826658	0.01517
NM_005908.4(MANBA):c.1485+23G>A	rs79449882	0.01200
NM_005908.4(MANBA):c.178-8A>G	rs113584126	0.01028
NM_005908.4(MANBA):c.1705-13C>A	rs34754408
NM_005908.4(MANBA):c.1705-13C>T	rs34754408
NM_005908.4(MANBA):c.2102C>T (p.Thr701Met)	rs2866413
NM_005908.4(MANBA):c.2416-10del	rs5860729

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