List of variants in gene combination LOC130056177, POMT2 reported as likely benign for 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

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.12C>T (p.Ala4=)
NM_013382.7(POMT2):c.25C>T (p.Leu9=)	rs1280735533
NM_013382.7(POMT2):c.30A>G (p.Ala10=)	rs2139552052
NM_013382.7(POMT2):c.6G>C (p.Pro2=)
NM_013382.7(POMT2):c.9G>A (p.Pro3=)	rs1594813347

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