List of variants reported as benign for Migraine, familial hemiplegic, 2 by Illumina Laboratory Services, Illumina

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.*2259T>A	rs3747625	0.21913
NM_000702.4(ATP1A2):c.*1026A>G	rs2070704	0.21697
NM_000702.4(ATP1A2):c.*1095T>A	rs56199408	0.21686
NM_000702.4(ATP1A2):c.*1629T>C	rs1046995	0.21680
NM_000702.4(ATP1A2):c.*746C>T	rs62620182	0.21625
NM_000702.4(ATP1A2):c.*748C>T	rs2070703	0.21623
NM_000702.4(ATP1A2):c.*589G>C	rs2070702	0.20323
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=)	rs1063125	0.18359
NM_000702.4(ATP1A2):c.3034+14C>T	rs41288127	0.13198
NM_000702.4(ATP1A2):c.*686G>A	rs55843060	0.12407
NM_000702.4(ATP1A2):c.*1548C>T	rs56003400	0.10471
NM_000702.4(ATP1A2):c.*1547G>T	rs55845795	0.10469
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=)	rs17846715	0.09246
NM_000702.4(ATP1A2):c.*1280G>A	rs4656884	0.05514
NM_000702.4(ATP1A2):c.*621A>G	rs12077973	0.03640
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=)	rs17846714	0.03612
NM_000702.4(ATP1A2):c.*253C>T	rs78930771	0.03535
NM_000702.4(ATP1A2):c.*546G>A	rs62621782	0.03531
NM_000702.4(ATP1A2):c.1652-11C>G	rs17846713	0.03344
NM_000702.4(ATP1A2):c.2961C>T (p.Cys987=)	rs74123254	0.02789
NM_000702.4(ATP1A2):c.*682T>C	rs60949592	0.02374
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=)	rs61734529	0.02220
NM_000702.4(ATP1A2):c.*1780G>A	rs74123255	0.02185
NM_000702.4(ATP1A2):c.*703G>A	rs57902482	0.01488
NM_000702.4(ATP1A2):c.*1284C>T	rs78507938	0.01486
NM_000702.4(ATP1A2):c.*72G>A	rs2070701	0.00654
NM_000702.4(ATP1A2):c.*1781C>T	rs116744472	0.00585
NM_000702.4(ATP1A2):c.-48C>G	rs41265761	0.00414
NM_000702.4(ATP1A2):c.2943-15C>T	rs111510835	0.00350
NM_000702.4(ATP1A2):c.*1000T>G	rs116194737	0.00242
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=)	rs138826759	0.00235
NM_000702.4(ATP1A2):c.2115+14C>T	rs200854586	0.00168
NM_000702.4(ATP1A2):c.*1355C>T	rs190096000	0.00166
NM_000702.4(ATP1A2):c.*1212G>C	rs558677583	0.00126
NM_000702.4(ATP1A2):c.*86G>A	rs368064571	0.00099
NM_000702.4(ATP1A2):c.*482A>C	rs373029091	0.00097
NM_000702.4(ATP1A2):c.2563+4C>T	rs3747626	0.00081
NM_000702.4(ATP1A2):c.*142A>G	rs117680524	0.00026
NM_000702.4(ATP1A2):c.194G>T (p.Arg65Leu)	rs187733403	0.00019
NM_000702.4(ATP1A2):c.2877G>A (p.Thr959=)	rs200127278	0.00001
NM_000702.4(ATP1A2):c.*1211C>A	rs62621216
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=)	rs537472446
NM_000702.4(ATP1A2):c.2564-8A>G	rs554846350

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