List of variants reported as uncertain significance for mirror movements 1 and/or agenesis of the corpus callosum

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.2105A>G (p.Asn702Ser)	rs35691189	0.00284
NM_005215.4(DCC):c.2624C>T (p.Thr875Met)	rs747051148	0.00003
GRCh38/hg38 18q21.2(chr18:53157259-53340005)x1
NM_005215.4(DCC):c.2220CAT[2] (p.Ile742del)
NM_005215.4(DCC):c.2227A>T (p.Met743Leu)	rs199651452
NM_005215.4(DCC):c.2316_2317delinsAA (p.Arg773Ser)	rs2057635830
NM_005215.4(DCC):c.2407G>A (p.Gly803Arg)	rs797044550
NM_005215.4(DCC):c.3620-2A>G	rs1292231805
Single allele

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