ClinVar Miner

Submissions for variant NM_001029896.2(WDR45):c.236-1G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Matlow's Ophthalmo-genetic Laboratory, Assaf Harofe Medical Center RCV003147747 SCV002569139 likely pathogenic Optic atrophy 2 no assertion criteria provided research

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