List of variants reported as uncertain significance for Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A; Usher syndrome type 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.2419G>A (p.Gly807Ser)	rs142652588	0.00011
NM_153676.4(USH1C):c.2192G>A (p.Arg731Gln)	rs371626423	0.00006
NM_153676.4(USH1C):c.361G>A (p.Gly121Ser)	rs377510653	0.00006
NM_153676.4(USH1C):c.1793G>A (p.Arg598His)	rs767863235	0.00004
NM_153676.4(USH1C):c.188G>A (p.Arg63Gln)	rs372497947	0.00004
NM_153676.4(USH1C):c.2377C>T (p.His793Tyr)	rs372227474	0.00004
NM_153676.4(USH1C):c.2374C>T (p.Arg792Trp)	rs200428926	0.00003
NM_153676.4(USH1C):c.1183C>T (p.His395Tyr)	rs769984840	0.00002
NM_153676.4(USH1C):c.793G>A (p.Asp265Asn)	rs199537187	0.00002
NM_153676.4(USH1C):c.152A>G (p.Asn51Ser)	rs775363189	0.00001
NM_153676.4(USH1C):c.2270G>A (p.Arg757His)	rs753703742	0.00001
NM_153676.4(USH1C):c.-60T>G	rs371444878

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