List of variants in gene CEP97 reported as benign for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_024548.4(CEP97):c.2538G>A (p.Gln846=)	rs2625282	0.90199
NM_024548.4(CEP97):c.955G>C (p.Val319Leu)	rs59720918	0.01320
NM_024548.4(CEP97):c.176G>A (p.Arg59Gln)	rs111912421	0.00410
NM_024548.4(CEP97):c.2022C>T (p.Ser674=)	rs75383743	0.00389
NM_024548.4(CEP97):c.840A>T (p.Leu280=)	rs2926543	0.00213
NM_024548.4(CEP97):c.1308A>G (p.Ala436=)	rs146247413	0.00093
NM_024548.4(CEP97):c.310C>T (p.Leu104=)	rs145437722	0.00052
NM_024548.4(CEP97):c.1400T>A (p.Met467Lys)	rs183786171	0.00030
NM_024548.4(CEP97):c.1089G>A (p.Ala363=)
NM_024548.4(CEP97):c.1282T>G (p.Leu428Val)	rs77015203
NM_024548.4(CEP97):c.1764C>A (p.Ile588=)
NM_024548.4(CEP97):c.187-17_187-16del	rs3070526
NM_024548.4(CEP97):c.44-13G>A
NM_024548.4(CEP97):c.690C>G (p.Leu230=)

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