List of variants in gene LAMA2 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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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_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser)	rs34367843	0.00914
NM_000426.4(LAMA2):c.4437-5T>A	rs41285288	0.00557
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp)	rs118147866	0.00549
NM_000426.4(LAMA2):c.5909G>C (p.Cys1970Ser)	rs148451013	0.00314
NM_000426.4(LAMA2):c.74C>T (p.Pro25Leu)	rs145310035	0.00147
NM_000426.4(LAMA2):c.3296A>G (p.Asn1099Ser)	rs35065563
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser)	rs56173620

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