ClinVar Miner

List of variants reported as likely benign for RD3-related retinopathy by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001164688.2(RD3):c.*1281G>A rs73072853 0.05356
NM_001164688.2(RD3):c.*2503G>T rs41309617 0.03264
NM_183059.2(RD3):c.-516T>G rs73069876 0.01335
NM_001164688.2(RD3):c.584A>T (p.Asp195Val) rs143207434 0.01101
NM_001164688.2(RD3):c.*1039T>A rs58551885 0.00911
NM_001164688.2(RD3):c.-294A>C rs202137622 0.00564
NM_001164688.2(RD3):c.*834G>A rs61849030
NM_001164688.2(RD3):c.*834G>T rs61849030

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