List of variants in gene combination LAMA2, LOC126859784 reported as pathogenic 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_000426.3(LAMA2):c.[2461A>C;8282T>C]
NM_000426.4(LAMA2):c.8245-2A>C
NM_000426.4(LAMA2):c.8245-2A>G	rs914395925
NM_000426.4(LAMA2):c.8256del (p.Ala2753fs)
NM_000426.4(LAMA2):c.8265del (p.Glu2756fs)
NM_000426.4(LAMA2):c.8297dup (p.Gly2767fs)	rs2114888851
NM_000426.4(LAMA2):c.8357+1G>A	rs1785749704

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