ClinVar Miner

Submissions for variant NM_013382.7(POMT2):c.636G>A (p.Lys212=)

gnomAD frequency: 0.00001  dbSNP: rs368906346
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001413055 SCV001615160 likely benign Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2; Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2; Autosomal recessive limb-girdle muscular dystrophy type 2N 2025-01-27 criteria provided, single submitter clinical testing

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