ClinVar Miner

Submissions for variant NM_001080442.3(SLC38A8):c.1214+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
Payam Genetics Center, General Welfare Department of North Khorasan Province RCV003159269 SCV003852668 uncertain significance Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome 2023-03-01 no assertion criteria provided clinical testing

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