List of variants in gene combination ATP1A2, LOC126805890 reported as pathogenic for Familial hemiplegic migraine

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.524del (p.Lys175fs)
NM_000702.4(ATP1A2):c.580G>T (p.Gly194Ter)
NM_000702.4(ATP1A2):c.605G>A (p.Arg202Gln)
NM_000702.4(ATP1A2):c.720_721del (p.Ile240fs)	rs2101986777
NM_000702.4(ATP1A2):c.736_739del (p.Asn246fs)	rs1651548761

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