List of variants in gene AP1S2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001272071.2(AP1S2):c.289-8C>T	rs770199415	0.00016
NM_001272071.2(AP1S2):c.-12C>T
NM_001272071.2(AP1S2):c.108G>A (p.Gln36=)
NM_001272071.2(AP1S2):c.112G>A (p.Val38Ile)

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