List of variants in gene combination EYS, PHF3 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001142800.2(EYS):c.9030A>G (p.Ala3010=)	rs61754905	0.01277
NM_001142800.2(EYS):c.8422G>A (p.Ala2808Thr)	rs111991705	0.00667
NM_001142800.2(EYS):c.8429C>T (p.Thr2810Ile)	rs144513453	0.00443
NM_001142800.2(EYS):c.9237A>G (p.Leu3079=)	rs139944387	0.00026
NM_001142800.2(EYS):c.9209T>C (p.Ile3070Thr)	rs183589498	0.00013
NM_001142800.2(EYS):c.9342TGT[1] (p.Val3116del)	rs536788112

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