ClinVar Miner

List of variants studied for Leber congenital amaurosis 12 by GeneReviews

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001164688.2(RD3):c.296+1G>A rs386834260

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