List of variants in gene LAMA1 reported as likely benign for ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005559.4(LAMA1):c.1183C>T (p.Arg395Cys)	rs148751644	0.00282
NM_005559.4(LAMA1):c.5481A>G (p.Val1827=)	rs138711280	0.00201
NM_005559.4(LAMA1):c.4554C>T (p.His1518=)	rs145068849	0.00176
NM_005559.4(LAMA1):c.7446A>G (p.Leu2482=)	rs145257845	0.00144
NM_005559.4(LAMA1):c.6066G>A (p.Ala2022=)	rs150951157	0.00101
NM_005559.4(LAMA1):c.4737C>T (p.Asn1579=)	rs201505782	0.00058
NM_005559.4(LAMA1):c.4204C>T (p.Pro1402Ser)	rs202133880	0.00024
NM_005559.4(LAMA1):c.8962C>T (p.Arg2988Cys)	rs138692442	0.00009
NM_005559.4(LAMA1):c.4555G>C (p.Gly1519Arg)	rs747710308	0.00003

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