List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1D; Pituitary adenoma 5, multiple types by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.7055-16A>G	rs4747193	0.34615
NM_022124.6(CDH23):c.1469G>C (p.Gly490Ala)	rs1227049	0.20047
NM_022124.6(CDH23):c.1449+130T>C	rs2305209	0.14152
NM_022124.6(CDH23):c.3625A>G (p.Thr1209Ala)	rs41281314	0.04612
NM_022124.6(CDH23):c.4858G>A (p.Val1620Met)	rs41281330	0.01037
NM_022124.6(CDH23):c.5418C>G (p.Asp1806Glu)	rs74145660

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