List of variants reported as uncertain significance for cardiac arrest

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.6206G>A (p.Arg2069His)	rs149645600	0.00065
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu)	rs113451409	0.00054
NM_005751.5(AKAP9):c.1099G>A (p.Val367Met)	rs138161478	0.00031
NM_001148.6(ANK2):c.5509G>A (p.Ala1837Thr)	rs199527708	0.00024
NM_017636.4(TRPM4):c.1069C>T (p.Arg357Trp)	rs764690335	0.00007
NM_201596.3(CACNB2):c.1206+3A>T	rs200174877	0.00006
NM_005751.5(AKAP9):c.1067A>T (p.Asp356Val)	rs533277424	0.00005
NM_001148.6(ANK2):c.7458C>G (p.His2486Gln)	rs776972443	0.00004
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr)	rs201046640	0.00004
NM_005477.3(HCN4):c.2197G>A (p.Val733Ile)	rs376631391	0.00004
NM_201596.3(CACNB2):c.1642G>A (p.Gly548Ser)	rs730880059	0.00004
NM_004415.4(DSP):c.2047G>A (p.Glu683Lys)	rs775181391	0.00003
NM_001148.6(ANK2):c.7577C>T (p.Ser2526Leu)	rs762909298	0.00002
NM_000335.5(SCN5A):c.559A>G (p.Thr187Ala)	rs869025517	0.00001
NM_001035.3(RYR2):c.378T>A (p.Ser126Arg)	rs869025507	0.00001
NM_002471.4(MYH6):c.4713G>T (p.Lys1571Asn)	rs730880151	0.00001
NM_004415.4(DSP):c.2260G>A (p.Glu754Lys)	rs730880080	0.00001
NM_004415.4(DSP):c.7249G>T (p.Asp2417Tyr)	rs760501352	0.00001
NM_005751.5(AKAP9):c.11378C>G (p.Ser3793Cys)	rs730880044	0.00001
NM_000335.5(SCN5A):c.5072T>C (p.Phe1691Ser)	rs869025521
NM_001035.3(RYR2):c.13759A>C (p.Ile4587Leu)	rs730880198
NM_001377540.1(SLMAP):c.2020+1G>A	rs869025527
NM_001943.5(DSG2):c.2188A>G (p.Thr730Ala)	rs780650226
NM_003803.4(MYOM1):c.3708C>A (p.Ser1236Arg)	rs869025489
NM_004982.4(KCNJ8):c.83G>C (p.Arg28Pro)	rs768851540
NM_005751.5(AKAP9):c.11276C>T (p.Pro3759Leu)	rs869025356
NM_014000.3(VCL):c.1559G>A (p.Arg520Gln)	rs757009736
NM_130797.4(DPP6):c.1039G>A (p.Ala347Thr)	rs770646362
NM_201596.3(CACNB2):c.1594T>G (p.Ser532Ala)	rs869025371

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