List of variants in gene PRKAG2 reported as likely benign for heart conduction disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_016203.4(PRKAG2):c.*3G>A	rs113234987	0.00973
NM_016203.4(PRKAG2):c.*384C>T	rs75418446	0.00847
NM_016203.4(PRKAG2):c.*56G>A	rs141781827	0.00626
NM_016203.4(PRKAG2):c.*572G>A	rs78192883	0.00384
NM_016203.4(PRKAG2):c.1593G>A (p.Arg531=)	rs148197254	0.00374
NM_016203.4(PRKAG2):c.111T>A (p.Ile37=)	rs144426409	0.00259
NM_016203.4(PRKAG2):c.1098A>G (p.Pro366=)	rs116541276	0.00169
NM_016203.4(PRKAG2):c.1704G>A (p.Thr568=)	rs138167675	0.00150
NM_016203.4(PRKAG2):c.298G>A (p.Gly100Ser)	rs79474211	0.00144
NM_016203.4(PRKAG2):c.*135T>C	rs184932311	0.00041
NM_016203.4(PRKAG2):c.147C>T (p.Asp49=)	rs761196275	0.00005
NM_016203.4(PRKAG2):c.297C>T (p.Pro99=)	rs767950372	0.00003
NM_016203.4(PRKAG2):c.*1021del	rs11329945
NM_016203.4(PRKAG2):c.*399G>A	rs112179332
NM_016203.4(PRKAG2):c.-287C>G	rs75059373
NM_016203.4(PRKAG2):c.1106+19del	rs374874465

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