List of variants in gene NEXMIF reported as pathogenic by OMIM

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.1441C>T (p.Arg481Ter)	rs886041701
NM_001008537.3(NEXMIF):c.1582del (p.Arg528fs)	rs727503977
NM_001008537.3(NEXMIF):c.183del (p.Arg62fs)	rs397518479
NM_001008537.3(NEXMIF):c.2042del (p.Gly681fs)	rs1556016555
NM_001008537.3(NEXMIF):c.3597dup (p.Ser1200fs)	rs397518478
NM_001008537.3(NEXMIF):c.438C>A (p.Cys146Ter)	rs1556016802
NM_001008537.3(NEXMIF):c.964C>T (p.Arg322Ter)	rs1556016731

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