List of variants in gene combination DNM2, LOC130063529 reported as uncertain significance for hereditary skeletal muscle disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.-116C>T	rs966672075	0.00004
NM_001005361.3(DNM2):c.-153G>T	rs886054138	0.00001
NM_001005361.3(DNM2):c.-122G>A	rs886054139
NM_001005361.3(DNM2):c.-19G>T	rs753599004
NM_001005361.3(DNM2):c.161G>A (p.Arg54Gln)
NM_001005361.3(DNM2):c.37G>C (p.Val13Leu)
NM_001005361.3(DNM2):c.4G>A (p.Gly2Ser)	rs2068817566

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