ClinVar Miner

List of variants studied for arrhythmogenic right ventricular dysplasia 2 by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (2):
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Total variants: 14
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HGVS dbSNP
NM_001035.3(RYR2):c.10361G>A (p.Arg3454His) rs1229045575
NM_001035.3(RYR2):c.1166G>A (p.Arg389His) rs200685968
NM_001035.3(RYR2):c.12541G>A (p.Gly4181Arg) rs775477470
NM_001035.3(RYR2):c.1258C>T (p.Arg420Trp) rs190140598
NM_001035.3(RYR2):c.13370A>G (p.Lys4457Arg) rs747584325
NM_001035.3(RYR2):c.14048_14049delinsAT (p.Arg4683Asn) rs1558439258
NM_001035.3(RYR2):c.1423A>C (p.Lys475Gln) rs765389300
NM_001035.3(RYR2):c.2320C>A (p.Pro774Thr) rs780965490
NM_001035.3(RYR2):c.2755G>A (p.Val919Met) rs201079716
NM_001035.3(RYR2):c.3660T>A (p.Asp1220Glu) rs1019112544
NM_001035.3(RYR2):c.4465T>C (p.Cys1489Arg) rs200450676
NM_001035.3(RYR2):c.5585A>G (p.Asp1862Gly) rs1559117209
NM_001035.3(RYR2):c.6320C>T (p.Thr2107Met) rs370331492
NM_001035.3(RYR2):c.8617C>T (p.Pro2873Ser) rs1031049689

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