List of variants in gene LAMA2 reported as not provided 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val)	rs147077184	0.00338
NM_000426.4(LAMA2):c.4010A>G (p.His1337Arg)	rs139739075	0.00024
NM_000426.4(LAMA2):c.4969G>A (p.Val1657Met)	rs370971334	0.00014
NM_000426.4(LAMA2):c.409G>A (p.Ala137Thr)	rs368349321	0.00006
NM_000426.4(LAMA2):c.5158G>C (p.Glu1720Gln)	rs760572086	0.00006
NM_000426.4(LAMA2):c.1854_1861dup (p.Leu621fs)	rs202247791	0.00001
NM_000426.4(LAMA2):c.2901C>A (p.Cys967Ter)	rs121913577	0.00001
NM_000426.4(LAMA2):c.1657C>T (p.Arg553Ter)	rs1303773212
NM_000426.4(LAMA2):c.2049_2050del (p.Arg683fs)	rs202247790
NM_000426.4(LAMA2):c.3068G>T (p.Cys1023Phe)	rs1773498113
NM_000426.4(LAMA2):c.370G>T (p.Val124Leu)	rs1278777348
NM_000426.4(LAMA2):c.7881T>G (p.His2627Gln)	rs202247792

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