ClinVar Miner

List of variants in gene MN1 reported as likely benign by GeneDx

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002430.3(MN1):c.1146G>T (p.Gln382His)	rs45589338	0.02685
NM_002430.3(MN1):c.1599A>G (p.Gln533=)	rs45480998	0.01026

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