List of variants in gene AP1S2 reported 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
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001272071.2(AP1S2):c.-12C>T	rs756612753	0.00039
NM_001272071.2(AP1S2):c.289-8C>T	rs770199415	0.00016
NM_001272071.2(AP1S2):c.112G>A (p.Val38Ile)	rs200944886	0.00008
NM_001272071.2(AP1S2):c.240G>A (p.Leu80=)	rs912444495	0.00001
NM_001272071.2(AP1S2):c.108G>A (p.Gln36=)	rs1934206938
NM_001272071.2(AP1S2):c.178dup (p.Arg60fs)	rs1934205000
NM_001272071.2(AP1S2):c.288+5G>A	rs587776739

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