List of variants in gene AP1S2 reported as uncertain significance by Ambry Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001272071.2(AP1S2):c.*1C>T	rs1016898604	0.00001
NM_001272071.2(AP1S2):c.244A>G (p.Ile82Val)	rs1399162998	0.00001
NM_001272071.2(AP1S2):c.107A>G (p.Gln36Arg)
NM_001272071.2(AP1S2):c.160C>G (p.Leu54Val)	rs2519929465
NM_001272071.2(AP1S2):c.373A>C (p.Thr125Pro)

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