ClinVar Miner

List of variants reported as likely benign for arrhythmogenic right ventricular dysplasia 9

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001267550.2(TTN):c.59113C>T (p.Arg19705Cys) rs72646839
NM_004572.3(PKP2):c.1012A>G (p.Thr338Ala) rs139851304
NM_004572.3(PKP2):c.1034+10C>T rs759397762
NM_004572.3(PKP2):c.1080C>T (p.Leu360=) rs397516984
NM_004572.3(PKP2):c.1104C>G (p.Ser368=) rs892666132
NM_004572.3(PKP2):c.1171-10T>C rs200122872
NM_004572.3(PKP2):c.1171-11T>C rs183414126
NM_004572.3(PKP2):c.1230C>T (p.Asp410=) rs148364390
NM_004572.3(PKP2):c.1326G>A (p.Leu442=) rs377076035
NM_004572.3(PKP2):c.1511-18A>G rs113698150
NM_004572.3(PKP2):c.156G>A (p.Lys52=) rs201210997
NM_004572.3(PKP2):c.1577C>T (p.Thr526Met) rs146882581
NM_004572.3(PKP2):c.1596C>T (p.Ile532=) rs145387575
NM_004572.3(PKP2):c.1629C>T (p.Tyr543=) rs765139046
NM_004572.3(PKP2):c.165G>T (p.Arg55=) rs1472609900
NM_004572.3(PKP2):c.1671C>T (p.Asn557=) rs535581825
NM_004572.3(PKP2):c.195C>T (p.Ala65=) rs397517014
NM_004572.3(PKP2):c.2130G>T (p.Thr710=) rs371089832
NM_004572.3(PKP2):c.2133C>T (p.Ala711=) rs529442984
NM_004572.3(PKP2):c.2253G>A (p.Ser751=) rs139098675
NM_004572.3(PKP2):c.2300-11del rs746936605
NM_004572.3(PKP2):c.2300-20dup rs746936605
NM_004572.3(PKP2):c.2349G>A (p.Pro783=) rs753226330
NM_004572.3(PKP2):c.2365A>G (p.Ile789Val) rs551045165
NM_004572.3(PKP2):c.2431C>A (p.Arg811Ser) rs139734328
NM_004572.3(PKP2):c.2489+12_2489+13insC rs1555141019
NM_004572.3(PKP2):c.419C>T (p.Ser140Phe) rs150821281
NM_004572.3(PKP2):c.505A>G (p.Ser169Gly) rs139139859
NM_004572.3(PKP2):c.888C>T (p.His296=) rs397517029
NM_004572.3(PKP2):c.903G>A (p.Leu301=) rs934225556
NM_004572.3(PKP2):c.951G>A (p.Ala317=) rs61729382
NM_004572.3(PKP2):c.978A>G (p.Ala326=) rs775137004

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