List of variants reported as uncertain significance for obsolete sudden cardiac death by Blueprint Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.5369T>G (p.Val1790Gly)	rs151021935	0.00082
NM_001035.3(RYR2):c.3380A>G (p.Glu1127Gly)	rs200525962	0.00048
NM_015141.4(GPD1L):c.520G>A (p.Glu174Lys)	rs112122950	0.00034
NM_001276345.2(TNNT2):c.720-4G>T	rs201753429	0.00009
NM_017636.4(TRPM4):c.1826C>G (p.Ala609Gly)	rs547541099	0.00006
NM_000257.4(MYH7):c.3853+1G>A	rs202031879	0.00002
NM_003803.4(MYOM1):c.3190C>T (p.His1064Tyr)	rs755409090	0.00002
NM_001148.6(ANK2):c.9173G>A (p.Arg3058His)	rs730880048	0.00001
NM_000719.7(CACNA1C):c.5626A>G (p.Lys1876Glu)	rs869025368
NM_000719.7(CACNA1C):c.985G>A (p.Gly329Ser)	rs786205744
NM_001040151.2(SCN3B):c.587C>G (p.Ser196Cys)	rs777776827
NM_006393.3(NEBL):c.2616G>T (p.Lys872Asn)	rs869025491
NM_130797.4(DPP6):c.674C>T (p.Pro225Leu)	rs869025384

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