ClinVar Miner

List of variants reported as uncertain significance for Retinitis pigmentosa; Retinitis pigmentosa 61; Usher syndrome type 3A by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_174878.3(CLRN1):c.218A>G (p.Gln73Arg)	rs201008540	0.00016
NM_174878.3(CLRN1):c.322C>T (p.Leu108Phe)	rs144691725	0.00005
NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg)	rs904836940	0.00001

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