List of variants in gene AIP reported as benign

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: 31

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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
NM_003977.4(AIP):c.*64G>A	rs115346238	0.00596
NM_003977.4(AIP):c.*60G>C	rs146014363	0.00566
NM_003977.4(AIP):c.891C>A (p.Ala297=)	rs35665586	0.00545
NM_003977.4(AIP):c.68G>A (p.Gly23Glu)	rs116940576	0.00115
NM_003977.4(AIP):c.911G>A (p.Arg304Gln)	rs104894190	0.00115
NM_003977.4(AIP):c.-84C>G	rs540839310	0.00086
NM_003977.4(AIP):c.301G>A (p.Val101Met)	rs147931650	0.00085
NM_003977.4(AIP):c.-23A>G	rs200665479	0.00064
NM_003977.4(AIP):c.382C>T (p.Arg128Cys)	rs140530307	0.00054
NM_003977.4(AIP):c.693G>A (p.Thr231=)	rs141715817	0.00046
NM_003977.4(AIP):c.36G>A (p.Gly12=)	rs79662690	0.00038
NM_003977.4(AIP):c.517G>A (p.Glu173Lys)	rs138902236	0.00034
NM_003977.4(AIP):c.753G>A (p.Leu251=)	rs147351993	0.00016
NM_003977.4(AIP):c.403C>T (p.His135Tyr)	rs150487522	0.00006
NM_003977.4(AIP):c.486G>A (p.Thr162=)	rs555078670	0.00005
NM_003977.4(AIP):c.696G>A (p.Pro232=)	rs780232812	0.00005
NM_003977.4(AIP):c.692C>T (p.Thr231Met)	rs532170807	0.00004
NM_003977.4(AIP):c.591G>A (p.Glu197=)	rs202006716	0.00003
NM_003977.4(AIP):c.366C>T (p.Cys122=)	rs748883061	0.00002
NM_003977.4(AIP):c.571C>T (p.Arg191Cys)	rs189861025	0.00001
NM_003977.4(AIP):c.72G>C (p.Glu24Asp)	rs201958318	0.00001
NC_000011.10:g.67482773dup	rs201817175
NM_003977.4(AIP):c.280-383dup
NM_003977.4(AIP):c.468+111C>T	rs4084113
NM_003977.4(AIP):c.469-147_469-144dup	rs5792416
NM_003977.4(AIP):c.645+23dup

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