ClinVar Miner

List of variants in gene LCA5 reported as likely benign for Leber congenital amaurosis 1

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_001122769.3(LCA5):c.*1528G>A rs41269343
NM_001122769.3(LCA5):c.*223A>G rs2292109
NM_001122769.3(LCA5):c.1967G>A (p.Gly656Asp) rs1875845
NM_001122769.3(LCA5):c.77A>C (p.Asp26Ala) rs34068461

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