List of variants reported as uncertain significance for alternating hemiplegia of childhood by Fulgent Genetics, Fulgent Genetics

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Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_152296.5(ATP1A3):c.-148T>G	rs769525784	0.00026
NM_000702.4(ATP1A2):c.1262G>A (p.Arg421Gln)	rs139499540	0.00014
NM_152296.5(ATP1A3):c.-64A>G	rs373531937	0.00006
NM_000475.5(NR0B1):c.315G>C (p.Trp105Cys)	rs132630327	0.00005
NM_000475.5(NR0B1):c.59C>G (p.Ala20Gly)	rs745852247	0.00001
NM_000475.5(NR0B1):c.697G>A (p.Ala233Thr)	rs761762294	0.00001
NM_000702.4(ATP1A2):c.1282C>T (p.Arg428Cys)	rs779985796	0.00001
NM_000702.4(ATP1A2):c.1550C>A (p.Thr517Asn)	rs749326394	0.00001
NM_000702.4(ATP1A2):c.1690C>T (p.Arg564Trp)	rs762330744	0.00001
NM_000702.4(ATP1A2):c.192G>T (p.Gln64His)	rs796052282	0.00001
NM_000702.4(ATP1A2):c.2062G>T (p.Ala688Ser)	rs200425518	0.00001
NM_000702.4(ATP1A2):c.2675T>C (p.Met892Thr)	rs794727222	0.00001
NM_152296.5(ATP1A3):c.2968G>A (p.Val990Ile)	rs781786336	0.00001
NM_000475.5(NR0B1):c.307_308delinsTT (p.Pro103Leu)	rs1569269085
NM_000475.5(NR0B1):c.593_594delinsAA (p.Arg198Gln)	rs1569268891
NM_000702.4(ATP1A2):c.1097G>A (p.Gly366Asp)	rs1057518514
NM_000702.4(ATP1A2):c.1859C>G (p.Thr620Arg)	rs1057521886
NM_000702.4(ATP1A2):c.2680G>T (p.Asp894Tyr)	rs1553245907
NM_000702.4(ATP1A2):c.2770G>A (p.Val924Met)	rs373276446
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr)	rs181618883
NM_152296.5(ATP1A3):c.-130GACG[3]	rs879996553

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