ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 62
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HGVS dbSNP
NM_004572.3(PKP2):c.1080C>T (p.Leu360=) rs397516984
NM_004572.3(PKP2):c.1093A>G (p.Met365Val) rs143900944
NM_004572.3(PKP2):c.1104C>G (p.Ser368=) rs892666132
NM_004572.3(PKP2):c.1114G>C (p.Ala372Pro) rs200586695
NM_004572.3(PKP2):c.1171-10T>C rs200122872
NM_004572.3(PKP2):c.1230C>T (p.Asp410=) rs148364390
NM_004572.3(PKP2):c.1251G>T (p.Gly417=) rs567854722
NM_004572.3(PKP2):c.12C>T (p.Pro4=) rs397516991
NM_004572.3(PKP2):c.1326G>A (p.Leu442=) rs377076035
NM_004572.3(PKP2):c.1379-1G>A rs139159464
NM_004572.3(PKP2):c.1420G>A (p.Ala474Thr) rs138538072
NM_004572.3(PKP2):c.1421C>T (p.Ala474Val) rs373399921
NM_004572.3(PKP2):c.1433C>T (p.Ala478Val) rs144620127
NM_004572.3(PKP2):c.1449T>C (p.Thr483=) rs781397552
NM_004572.3(PKP2):c.1468C>T (p.Arg490Trp) rs149930872
NM_004572.3(PKP2):c.1482A>G (p.Ser494=) rs397516995
NM_004572.3(PKP2):c.1550A>G (p.Asn517Ser) rs144536197
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.1636G>A (p.Ala546Thr) rs368740836
NM_004572.3(PKP2):c.1759G>A (p.Val587Ile) rs146102241
NM_004572.3(PKP2):c.184C>A (p.Gln62Lys) rs199601548
NM_004572.3(PKP2):c.1866C>G (p.Leu622=) rs1460314882
NM_004572.3(PKP2):c.195C>T (p.Ala65=) rs397517014
NM_004572.3(PKP2):c.1989G>A (p.Pro663=) rs760434776
NM_004572.3(PKP2):c.198G>A (p.Arg66=) rs144106848
NM_004572.3(PKP2):c.2087A>G (p.Asn696Ser) rs140852019
NM_004572.3(PKP2):c.2130G>A (p.Thr710=) rs371089832
NM_004572.3(PKP2):c.2130G>T (p.Thr710=) rs371089832
NM_004572.3(PKP2):c.213C>T (p.Ser71=) rs1173618581
NM_004572.3(PKP2):c.2150C>T (p.Pro717Leu) rs144018320
NM_004572.3(PKP2):c.2151G>A (p.Pro717=) rs147995773
NM_004572.3(PKP2):c.2253G>A (p.Ser751=) rs139098675
NM_004572.3(PKP2):c.2300-10C>T rs1410924735
NM_004572.3(PKP2):c.2300-4G>C rs376231586
NM_004572.3(PKP2):c.2300-4G>T rs376231586
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.2433C>T (p.Arg811=) rs369166666
NM_004572.3(PKP2):c.2448C>T (p.Thr816=) rs369837002
NM_004572.3(PKP2):c.2487T>C (p.Asp829=) rs142362933
NM_004572.3(PKP2):c.2490-6T>C rs761613652
NM_004572.3(PKP2):c.2589G>A (p.Lys863=) rs777477467
NM_004572.3(PKP2):c.2619C>T (p.Ala873=) rs747191995
NM_004572.3(PKP2):c.387G>A (p.Gln129=) rs768974835
NM_004572.3(PKP2):c.406G>A (p.Val136Met) rs567795321
NM_004572.3(PKP2):c.419C>T (p.Ser140Phe) rs150821281
NM_004572.3(PKP2):c.45C>T (p.Thr15=) rs759214983
NM_004572.3(PKP2):c.486G>A (p.Thr162=) rs189040311
NM_004572.3(PKP2):c.505A>G (p.Ser169Gly) rs139139859
NM_004572.3(PKP2):c.576G>A (p.Pro192=) rs373380483
NM_004572.3(PKP2):c.771G>A (p.Glu257=) rs1060504159
NM_004572.3(PKP2):c.795G>T (p.Gly265=) rs375268778
NM_004572.3(PKP2):c.826C>T (p.Pro276Ser) rs201944276
NM_004572.3(PKP2):c.888C>T (p.His296=) rs397517029
NM_004572.3(PKP2):c.900G>A (p.Thr300=) rs140235564
NM_004572.3(PKP2):c.903G>A (p.Leu301=) rs934225556
NM_004572.3(PKP2):c.918C>T (p.Pro306=) rs368656084
NM_004572.3(PKP2):c.963C>T (p.Val321=) rs202207343
NM_004572.3(PKP2):c.975C>T (p.Ala325=) rs369921166
NM_004572.3(PKP2):c.978A>G (p.Ala326=) rs775137004

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