ClinVar Miner

List of variants reported as likely benign for Wolff-Parkinson-White syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_016203.3(PRKAG2):c.-560C>T rs117728810 0.04777
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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