List of variants reported as likely benign for Usher syndrome type 2A; Retinitis pigmentosa 39 by Fulgent Genetics, Fulgent Genetics

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_206933.4(USH2A):c.1931A>T (p.Asp644Val)	rs1805048	0.05002
NM_206933.4(USH2A):c.15377T>C (p.Ile5126Thr)	rs111033266	0.02380
NM_206933.4(USH2A):c.6713A>C (p.Glu2238Ala)	rs41277212	0.01940
NM_206933.4(USH2A):c.13763C>A (p.Ser4588Tyr)	rs78253373	0.00962
NM_206933.4(USH2A):c.11048-15C>T	rs74141403	0.00691
NM_206933.4(USH2A):c.9262G>A (p.Glu3088Lys)	rs56056328	0.00606
NM_206933.4(USH2A):c.10851C>T (p.Asn3617=)	rs12073994	0.00488
NM_206933.4(USH2A):c.9459C>T (p.Cys3153=)	rs73090721	0.00422
NM_206933.4(USH2A):c.14074G>A (p.Gly4692Arg)	rs45549044	0.00420
NM_206933.4(USH2A):c.8458G>A (p.Val2820Ile)	rs59174500	0.00394
NM_206933.4(USH2A):c.15433G>A (p.Val5145Ile)	rs111033269	0.00369
NM_206933.4(USH2A):c.3364T>G (p.Ser1122Ala)	rs148135241	0.00152
NM_206933.4(USH2A):c.4698G>A (p.Gln1566=)	rs143218330	0.00115
NM_206933.4(USH2A):c.2256T>C (p.His752=)	rs111033281	0.00098
NM_206933.4(USH2A):c.6628C>G (p.Pro2210Ala)	rs192115090	0.00086
NM_206933.4(USH2A):c.1966G>A (p.Asp656Asn)	rs146824138	0.00071
NM_206933.4(USH2A):c.15427C>T (p.Arg5143Cys)	rs145771342	0.00056
NM_206933.4(USH2A):c.4758+3A>G	rs117798425	0.00056
NM_206933.4(USH2A):c.6924A>G (p.Ala2308=)	rs148504065	0.00056
NM_206933.4(USH2A):c.8320G>A (p.Ala2774Thr)	rs111033533	0.00054
NM_206933.4(USH2A):c.9340C>T (p.Pro3114Ser)	rs201071654	0.00040
NM_206933.4(USH2A):c.6001C>T (p.Arg2001Cys)	rs141539554	0.00038
NM_206933.4(USH2A):c.9915G>C (p.Glu3305Asp)	rs145278250	0.00031
NM_206933.4(USH2A):c.7334C>T (p.Ser2445Phe)	rs41315579	0.00023
NM_206933.2(USH2A):c.3902G>T (p.Gly1301Val)	rs111033524	0.00008
NM_206933.4(USH2A):c.12743A>G (p.His4248Arg)	rs145830318

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