List of variants in gene combination LOC130056177, POMT2 reported as uncertain significance for Autosomal recessive limb-girdle muscular dystrophy type 2N

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.-142C>T	rs886050827	0.00068
NM_013382.7(POMT2):c.-149C>A	rs886050828	0.00010
NM_013382.7(POMT2):c.-113G>A	rs1891868176
NM_013382.7(POMT2):c.-136G>A	rs1891870150
NM_013382.7(POMT2):c.-172C>A	rs897215490
NM_013382.7(POMT2):c.-176C>G	rs978645827

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