List of variants reported as uncertain significance for Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005559.4(LAMA1):c.485G>A (p.Arg162His)	rs759415734	0.00011
NM_005559.4(LAMA1):c.4024G>C (p.Val1342Leu)	rs2144110328
NM_005559.4(LAMA1):c.7603G>A (p.Gly2535Ser)
NM_005559.4(LAMA1):c.9160T>C (p.Phe3054Leu)

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