List of variants in gene AIP reported as benign for endocrine gland neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_003977.4(AIP):c.920= (p.Arg307=)	rs4930199	0.99984
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.*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.-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.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.609C>T (p.Tyr203=)	rs146317385	0.00007
NM_003977.4(AIP):c.366C>T (p.Cys122=)	rs748883061	0.00002
NM_003977.4(AIP):c.571C>T (p.Arg191Cys)	rs189861025	0.00001

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