List of variants reported as uncertain significance for Lissencephaly by University of Washington Center for Mendelian Genomics, University of Washington

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10313G>A (p.Arg3438Gln)	rs1375729860	0.00001
NM_000430.4(PAFAH1B1):c.655T>G (p.Trp219Gly)	rs2069200834
NM_000430.4(PAFAH1B1):c.743T>C (p.Leu248Pro)	rs2069227815
NM_001376.5(DYNC1H1):c.10420C>T (p.Arg3474Trp)	rs757725348
NM_001376.5(DYNC1H1):c.10888G>A (p.Gly3630Ser)	rs2048578300
NM_001376.5(DYNC1H1):c.3161G>C (p.Trp1054Ser)	rs2048038170
NM_001376.5(DYNC1H1):c.4808G>C (p.Arg1603Thr)	rs1555409418
NM_001376.5(DYNC1H1):c.9954G>T (p.Lys3318Asn)	rs2048518511
NM_001614.5(ACTG1):c.535G>T (p.Asp179Tyr)	rs2031766655
NM_006009.4(TUBA1A):c.995T>C (p.Ile332Thr)	rs587784497
NM_178012.5(TUBB2B):c.73A>G (p.Ser25Gly)	rs1757291106
NM_178012.5(TUBB2B):c.747C>A (p.Asp249Glu)	rs1757274789

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