List of variants in gene AP3B1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003664.5(AP3B1):c.1969-10G>A	rs77009095	0.05363
NM_003664.5(AP3B1):c.1683C>T (p.Leu561=)	rs17192146	0.04676
NM_003664.5(AP3B1):c.1116G>C (p.Leu372=)	rs76433453	0.02452
NM_001271769.2(AP3B1):c.*588A>G	rs114954951	0.02413
NM_003664.5(AP3B1):c.687A>G (p.Leu229=)	rs35496909	0.01507
NM_003664.5(AP3B1):c.339A>C (p.Ala113=)	rs7706167	0.01450
NM_003664.5(AP3B1):c.2915A>G (p.Asn972Ser)	rs139968311	0.00213
NM_003664.5(AP3B1):c.1857T>G (p.Leu619=)	rs115892142	0.00200
NM_003664.5(AP3B1):c.942G>A (p.Ala314=)	rs146871001	0.00093
NM_003664.5(AP3B1):c.1367T>C (p.Ile456Thr)	rs536306260	0.00007
NM_003664.5(AP3B1):c.1421C>T (p.Ala474Val)	rs191850940	0.00001
NM_003664.5(AP3B1):c.2409_2411del (p.Lys804del)	rs199702315
NM_003664.5(AP3B1):c.2769A>C (p.Lys923Asn)	rs201179527
NM_003664.5(AP3B1):c.3020CTG[1] (p.Ala1008del)	rs111935323

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