List of variants in gene NEXMIF reported as likely pathogenic for not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 Xq13.3(chrX:74016853-74178303)x0
NC_000023.11:g.(?_74739385)_(74745670_?)dup
NM_001008537.3(NEXMIF):c.1123G>T (p.Glu375Ter)	rs1602212476
NM_001008537.3(NEXMIF):c.694C>T (p.Gln232Ter)	rs2080116822
NM_001008537.3(NEXMIF):c.864AGA[1] (p.Glu289del)

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