List of variants reported as uncertain significance for Catecholaminergic polymorphic ventricular tachycardia 1 by Blueprint Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013	0.00150
NM_170707.4(LMNA):c.1201C>T (p.Arg401Cys)	rs61094188	0.00015
NM_000335.5(SCN5A):c.52C>T (p.Arg18Trp)	rs199473044	0.00006
NM_017636.4(TRPM4):c.3512G>A (p.Arg1171His)	rs762615860	0.00003
NM_000256.3(MYBPC3):c.503T>C (p.Val168Ala)	rs727505267	0.00002
NM_001035.3(RYR2):c.9352G>A (p.Gly3118Arg)	rs730880194	0.00001
NM_001105206.3(LAMA4):c.2576C>T (p.Thr859Met)	rs730880121	0.00001
NM_001148.6(ANK2):c.11611G>A (p.Gly3871Arg)	rs786205729	0.00001
NM_004415.4(DSP):c.2597G>A (p.Arg866His)	rs764965132	0.00001
NM_000238.4(KCNH2):c.473-7C>G	rs146570628
NM_000256.3(MYBPC3):c.3118T>G (p.Ser1040Ala)	rs730880139
NM_000335.5(SCN5A):c.1840C>T (p.Pro614Ser)	rs730880204
NM_001035.3(RYR2):c.1604A>G (p.Glu535Gly)	rs869025509
NM_004409.5(DMPK):c.582-6G>C	rs766818029
NM_174934.4(SCN4B):c.592_593+1del	rs587782976

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