ClinVar Miner

List of variants in gene RD3 reported as pathogenic for Leber congenital amaurosis

Included ClinVar conditions (39):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_183059.2(RD3):c.112C>T (p.Arg38Ter) rs786205148
NM_183059.2(RD3):c.136G>T (p.Glu46Ter) rs786205150
NM_183059.2(RD3):c.137_138del (p.Glu46fs) rs786205149
NM_183059.2(RD3):c.180C>A (p.Tyr60Ter) rs762631020
NM_183059.2(RD3):c.296+1G>A rs386834260

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