ClinVar Miner

Submissions for variant NM_017739.4(POMGNT1):c.1398G>A (p.Trp466Ter)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003463349 SCV004205986 likely pathogenic Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 2023-05-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005030046 SCV005655822 likely pathogenic Autosomal recessive limb-girdle muscular dystrophy type 2O; Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3; Retinitis pigmentosa 76 2024-01-11 criteria provided, single submitter clinical testing

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