List of variants in gene NFIA reported as likely pathogenic by Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes

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_001134673.4(NFIA):c.106delinsTGAACCTGTATTGAAGTATTT (p.Arg36Ter)	rs1646255018
NM_001134673.4(NFIA):c.984_1015del (p.Lys328fs)	rs2100485780

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