List of variants in gene AVIL reported as likely pathogenic for familial nephrotic syndrome

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_006576.4(AVIL):c.404G>A (p.Arg135Gln)	rs138047529	0.00034
NM_006576.4(AVIL):c.595C>T (p.Arg199Ter)

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