List of variants in gene AVIL reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006576.4(AVIL):c.1204A>G (p.Ile402Val)	rs2140450849
NM_006576.4(AVIL):c.121G>A (p.Asp41Asn)
NM_006576.4(AVIL):c.1285A>G (p.Thr429Ala)
NM_006576.4(AVIL):c.431A>T (p.Asn144Ile)	rs2140456079
NM_006576.4(AVIL):c.66+9G>A
NM_006576.4(AVIL):c.812dup (p.Leu272fs)

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