List of variants studied for cerebral arterial disease by OMIM

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001256071.3(RNF213):c.14429G>A (p.Arg4810Lys)	rs112735431	0.00004
NM_001130682.3(GUCY1A1):c.1045C>T (p.Arg349Ter)	rs587777321	0.00001
NM_001130682.3(GUCY1A1):c.1258C>T (p.Arg420Ter)	rs373182378	0.00001
NM_001256071.3(RNF213):c.12037G>A (p.Asp4013Asn)	rs397514563	0.00001
NM_001613.4(ACTA2):c.772C>T (p.Arg258Cys)	rs121434528	0.00001
NM_001130682.3(GUCY1A1):c.1086+1G>A	rs587777320
NM_001130682.3(GUCY1A1):c.1170del (p.Glu391fs)	rs587777322
NM_001130682.3(GUCY1A1):c.1550G>A (p.Cys517Tyr)	rs751701114
NM_001130682.3(GUCY1A1):c.1954G>T (p.Gly652Ter)	rs1368733883
NM_001130682.3(GUCY1A1):c.334_335del (p.Glu112fs)	rs781020381
NM_001613.4(ACTA2):c.536G>A (p.Arg179His)	rs387906592
NM_001613.4(ACTA2):c.773G>A (p.Arg258His)	rs121434527
NM_018043.7(ANO1):c.1972A>G (p.Met658Val)
NM_018043.7(ANO1):c.2219C>T (p.Thr740Ile)
NM_018043.7(ANO1):c.508G>A (p.Glu170Lys)
NM_018676.4(THSD1):c.1348C>T (p.Arg450Ter)	rs1594095223

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