List of variants reported as uncertain significance for basal ganglia disorder by 3billion

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_018713.3(SLC30A10):c.1006C>T (p.His336Tyr)	rs770740586
NM_020702.5(MYORG):c.1086CTTCGA[1] (p.363FD[1])	rs1398218251
NM_020702.5(MYORG):c.1469A>G (p.Tyr490Cys)	rs2131878793
NM_020702.5(MYORG):c.1991C>T (p.Pro664Leu)	rs771434563
NM_020702.5(MYORG):c.954G>T (p.Trp318Cys)
NM_152296.5(ATP1A3):c.2128A>C (p.Asn710His)

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