List of variants in gene AP1S3 reported as likely benign for immune system disorder

Minimum submission review status:		Collection method:
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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_001039569.2(AP1S3):c.97C>T (p.Arg33Trp)	rs138292988	0.00725
NM_001039569.2(AP1S3):c.64A>G (p.Thr22Ala)	rs149183052	0.00120

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