List of variants reported as uncertain significance for Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_005559.4(LAMA1):c.2323G>A (p.Gly775Ser)	rs28369373	0.00028
NM_005559.4(LAMA1):c.7220A>G (p.Tyr2407Cys)	rs199811630	0.00013
NM_005559.4(LAMA1):c.3679G>A (p.Gly1227Arg)	rs776158943	0.00009
NM_005559.4(LAMA1):c.1280G>A (p.Cys427Tyr)
NM_005559.4(LAMA1):c.2750A>C (p.Glu917Ala)
NM_005559.4(LAMA1):c.4328C>A (p.Thr1443Asn)
NM_005559.4(LAMA1):c.7610G>A (p.Arg2537His)

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