List of variants reported as uncertain significance for Alternating hemiplegia of childhood 1; Migraine, familial hemiplegic, 2; Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies; Developmental and epileptic encephalopathy 98 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.1262G>A (p.Arg421Gln)	rs139499540	0.00014
NM_000702.4(ATP1A2):c.1550C>A (p.Thr517Asn)	rs749326394	0.00001
NM_000702.4(ATP1A2):c.1931G>A (p.Arg644Gln)	rs745824475	0.00001
NM_000702.4(ATP1A2):c.1859C>G (p.Thr620Arg)	rs1057521886

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