List of variants reported as uncertain significance for arrhythmogenic right ventricular cardiomyopathy by CSER _CC_NCGL, University of Washington

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly)	rs142841727	0.00439
NM_001005242.3(PKP2):c.1627G>A (p.Val543Ile)	rs146102241	0.00255
NM_001005242.3(PKP2):c.419C>T (p.Ser140Phe)	rs150821281	0.00252
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile)	rs193922639	0.00158
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013	0.00150
NM_024422.6(DSC2):c.2194T>G (p.Leu732Val)	rs151024019	0.00138
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965	0.00131
NM_001005242.3(PKP2):c.505A>G (p.Ser169Gly)	rs139139859	0.00096
NM_003239.5(TGFB3):c.293C>T (p.Ser98Leu)	rs142047577	0.00092
NM_024422.6(DSC2):c.304G>A (p.Glu102Lys)	rs144799937	0.00070
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr)	rs201500134	0.00069
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln)	rs149514924	0.00063
NM_001005242.3(PKP2):c.184C>A (p.Gln62Lys)	rs199601548	0.00041
NM_004415.4(DSP):c.1696G>A (p.Ala566Thr)	rs148147581	0.00026
NM_004415.4(DSP):c.2422C>T (p.Arg808Cys)	rs150339369	0.00021
NM_001943.5(DSG2):c.1912G>A (p.Gly638Arg)	rs201564919	0.00016
NM_024422.6(DSC2):c.2471C>T (p.Ser824Leu)	rs143413607	0.00016
NM_004415.4(DSP):c.242G>A (p.Cys81Tyr)	rs140965835	0.00014
NM_001005242.3(PKP2):c.1930T>C (p.Ser644Pro)	rs144601090	0.00011
NM_004415.4(DSP):c.6307A>G (p.Lys2103Glu)	rs149513743	0.00010
NM_001035.3(RYR2):c.5822G>A (p.Arg1941His)	rs373600053	0.00007
NM_001943.5(DSG2):c.2471G>A (p.Arg824His)	rs376858770	0.00005
NM_001005242.3(PKP2):c.1379-2022G>A	rs111450489	0.00004
NM_024422.6(DSC2):c.490G>A (p.Ala164Thr)	rs978623916	0.00004
NM_001943.5(DSG2):c.706A>G (p.Thr236Ala)	rs727502985	0.00003
NM_024422.6(DSC2):c.595C>T (p.Arg199Cys)	rs769787593	0.00003
NM_001035.3(RYR2):c.3484G>A (p.Val1162Met)	rs377030538	0.00002
NM_004415.4(DSP):c.5324G>T (p.Arg1775Ile)	rs34738426	0.00002
NM_001035.3(RYR2):c.11968G>A (p.Val3990Ile)	rs1210103464	0.00001
NM_001035.3(RYR2):c.12023A>G (p.Asn4008Ser)	rs1330847491	0.00001
NM_001035.3(RYR2):c.2402G>T (p.Arg801Leu)	rs371157868	0.00001
NM_001005242.3(PKP2):c.2299C>A (p.Arg767Ser)	rs139734328
NM_001035.3(RYR2):c.4196C>A (p.Thr1399Lys)	rs75901196

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