List of variants in gene AIP reported as 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003977.4(AIP):c.920= (p.Arg307=)	rs4930199	0.99984
NM_003977.4(AIP):c.469-236G>T	rs611697	0.84929
NM_003977.4(AIP):c.682C>A (p.Gln228Lys)	rs641081	0.84113
NM_003977.4(AIP):c.516C>T (p.Asp172=)	rs2276020	0.03152
NM_003977.4(AIP):c.468+244G>A	rs115215716	0.01912
NC_000011.10:g.67482773dup	rs201817175
NM_003977.4(AIP):c.468+111C>T	rs4084113
NM_003977.4(AIP):c.469-147_469-144dup	rs5792416

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