List of variants in gene AIP reported as likely benign by GeneDx

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003977.4(AIP):c.*60G>C	rs146014363	0.00566
NM_003977.4(AIP):c.468+136A>G	rs79270719	0.00513
NM_003977.4(AIP):c.47G>A (p.Arg16His)	rs145047094	0.00197
NM_003977.4(AIP):c.896C>T (p.Ala299Val)	rs148986773	0.00065
NM_003977.4(AIP):c.807C>T (p.Phe269=)	rs139407567	0.00055
NM_003977.4(AIP):c.753G>A (p.Leu251=)	rs147351993	0.00016
NM_003977.4(AIP):c.486G>A (p.Thr162=)	rs555078670	0.00005
NM_003977.4(AIP):c.787+9C>T	rs749392143	0.00004
NM_003977.4(AIP):c.788-29TGCCCAC[3]	rs540045132

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