ClinVar Miner

List of variants in gene AP3D1 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001261826.3(AP3D1):c.3233A>G (p.Lys1078Arg)	rs201804540	0.00025
NM_001261826.3(AP3D1):c.2601+6G>T	rs1265838305	0.00003

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