ClinVar Miner

List of variants in gene LCA5 reported as benign for Leber congenital amaurosis 5

Included ClinVar conditions (1):
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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001122769.3(LCA5):c.71T>C (p.Leu24Ser) rs2655655 0.84544
NM_001122769.3(LCA5):c.-62A>G rs2803195 0.84542
NM_001122769.3(LCA5):c.*223A>G rs2292109 0.45638
NM_001122769.3(LCA5):c.1967G>A (p.Gly656Asp) rs1875845 0.36167
NM_001122769.3(LCA5):c.77A>C (p.Asp26Ala) rs34068461 0.14840
NM_001122769.3(LCA5):c.-334C>T rs116580217 0.01110
NM_001122769.3(LCA5):c.*1292A>G rs77354230 0.01061

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