List of variants studied for electroclinical syndrome by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001191061.2(SLC25A22):c.412+10G>T	rs113091974	0.03661
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=)	rs61753382	0.00763
NM_001191061.2(SLC25A22):c.570C>T (p.Leu190=)	rs145322467	0.00137
NM_004171.4(SLC1A2):c.92G>A (p.Arg31Gln)	rs199599866	0.00020
NM_001130438.3(SPTAN1):c.7161-8G>A	rs202180736	0.00014
NM_001271.4(CHD2):c.4814A>C (p.Lys1605Thr)	rs780701076	0.00006
NM_001134407.3(GRIN2A):c.3884T>C (p.Ile1295Thr)	rs757351084	0.00004
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser)	rs74582884
NM_004519.4(KCNQ3):c.883G>C (p.Glu295Gln)
NM_020705.2(TBC1D24):c.[338C>A];[476T>C]

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