ClinVar Miner

List of variants studied for Brugada syndrome 2

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_015141.4(GPD1L):c.81T>C (p.Asn27=) rs34278284 0.00515
NM_015141.4(GPD1L):c.370A>G (p.Ile124Val) rs72552293 0.00291
NM_015141.4(GPD1L):c.981G>A (p.Val327=) rs144877595 0.00195
NM_015141.4(GPD1L):c.619-9C>G rs2044880 0.00057
NM_015141.4(GPD1L):c.520G>A (p.Glu174Lys) rs112122950 0.00034
NM_015141.4(GPD1L):c.813G>T (p.Arg271=) rs35464343 0.00031
NM_015141.4(GPD1L):c.459C>T (p.Asn153=) rs375532052 0.00019
NM_015141.4(GPD1L):c.247G>A (p.Glu83Lys) rs72552292 0.00018
NM_015141.4(GPD1L):c.1038C>T (p.Ser346=) rs147092668 0.00016
NM_015141.4(GPD1L):c.467A>G (p.Asn156Ser) rs139494055 0.00012
NM_015141.4(GPD1L):c.839C>T (p.Ala280Val) rs72552291 0.00011
NM_015141.4(GPD1L):c.959+11C>T rs370985609 0.00011
NM_015141.4(GPD1L):c.367-10A>T rs113764055 0.00006
NM_015141.4(GPD1L):c.658C>T (p.Arg220Cys) rs72546647 0.00006
NM_015141.4(GPD1L):c.367-11C>A rs113202696 0.00004
NM_015141.4(GPD1L):c.817C>T (p.Arg273Cys) rs72552294 0.00004
NM_015141.4(GPD1L):c.505+2T>G rs943929226 0.00003
NM_015141.4(GPD1L):c.775G>A (p.Gly259Arg) rs146477959 0.00003
NM_015141.4(GPD1L):c.158C>G (p.Thr53Arg) rs1053382446 0.00002
NM_015141.4(GPD1L):c.838G>A (p.Ala280Thr) rs764691105 0.00002
NM_015141.4(GPD1L):c.376del (p.Glu126fs) rs761698828 0.00001
NM_015141.4(GPD1L):c.415C>T (p.Arg139Cys) rs771369026 0.00001
NM_015141.4(GPD1L):c.416G>A (p.Arg139His) rs775043567 0.00001
NM_015141.4(GPD1L):c.482A>G (p.Glu161Gly) rs754861753 0.00001
NM_015141.4(GPD1L):c.505G>A (p.Gly169Ser) rs1446434571 0.00001
NM_015141.4(GPD1L):c.878T>C (p.Met293Thr) rs188138719 0.00001
NM_015141.4(GPD1L):c.905C>T (p.Pro302Leu) rs1409253059 0.00001
NM_015141.4(GPD1L):c.977C>A (p.Ala326Glu) rs774304068 0.00001
NM_015141.4(GPD1L):c.997G>A (p.Glu333Lys) rs201799095 0.00001
NM_015141.4(GPD1L):c.257A>G (p.Gln86Arg) rs755240955
NM_015141.4(GPD1L):c.367-11_367-10delinsAT rs1575115586
NM_015141.4(GPD1L):c.560A>G (p.Asn187Ser) rs951273802
NM_015141.4(GPD1L):c.619-9C>A rs2044880
NM_015141.4(GPD1L):c.853-2A>G rs766733448
NM_015141.4(GPD1L):c.914CTG[1] (p.Ala306del) rs2125498333

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