List of variants in gene AP2S1 reported as pathogenic for lung disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004069.6(AP2S1):c.43C>T (p.Arg15Cys)	rs397514498
NM_004069.6(AP2S1):c.44G>A (p.Arg15His)	rs397514499
NM_004069.6(AP2S1):c.44G>T (p.Arg15Leu)	rs397514499

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