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: 79
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HGVS dbSNP
NM_001005242.3(PKP2):c.1080C>T (p.Leu360=) rs397516984
NM_001005242.3(PKP2):c.1093A>G (p.Met365Val) rs143900944
NM_001005242.3(PKP2):c.1114G>C (p.Ala372Pro) rs200586695
NM_001005242.3(PKP2):c.1171-10T>C rs200122872
NM_001005242.3(PKP2):c.12C>T (p.Pro4=) rs397516991
NM_001005242.3(PKP2):c.1379-1967_1379-1966del
NM_001005242.3(PKP2):c.1379-1998C>A
NM_001005242.3(PKP2):c.1379-2002A>G
NM_001005242.3(PKP2):c.1379-2005A>G rs397516995
NM_001005242.3(PKP2):c.1379-2011G>C
NM_001005242.3(PKP2):c.1379-2019C>T rs149930872
NM_001005242.3(PKP2):c.1379-2054C>T rs144620127
NM_001005242.3(PKP2):c.1379-2067G>A rs138538072
NM_001005242.3(PKP2):c.1379-2071G>A
NM_001005242.3(PKP2):c.1379-2109G>A rs139159464
NM_001005242.3(PKP2):c.1418A>G (p.Asn473Ser) rs144536197
NM_001005242.3(PKP2):c.1476T>C (p.Ser492=)
NM_001005242.3(PKP2):c.1504G>A (p.Ala502Thr) rs368740836
NM_001005242.3(PKP2):c.1593G>A (p.Ala531=)
NM_001005242.3(PKP2):c.1627G>A (p.Val543Ile) rs146102241
NM_001005242.3(PKP2):c.1848G>A (p.Gln616=)
NM_001005242.3(PKP2):c.1955A>G (p.Asn652Ser) rs140852019
NM_001005242.3(PKP2):c.195C>T (p.Ala65=) rs397517014
NM_001005242.3(PKP2):c.2018C>T (p.Pro673Leu) rs144018320
NM_001005242.3(PKP2):c.2121G>A (p.Ser707=) rs139098675
NM_001005242.3(PKP2):c.2167+8G>A
NM_001005242.3(PKP2):c.2233A>G (p.Ile745Val) rs551045165
NM_001005242.3(PKP2):c.2299C>A (p.Arg767Ser) rs139734328
NM_001005242.3(PKP2):c.2355T>C (p.Asp785=) rs142362933
NM_001005242.3(PKP2):c.2446-11dup rs397517024
NM_001005242.3(PKP2):c.419C>T (p.Ser140Phe) rs150821281
NM_001005242.3(PKP2):c.473G>A (p.Arg158Lys) rs397517027
NM_001005242.3(PKP2):c.505A>G (p.Ser169Gly) rs139139859
NM_001005242.3(PKP2):c.558C>T (p.Ala186=) rs184522105
NM_001005242.3(PKP2):c.696C>T (p.Asp232=) rs375677250
NM_001005242.3(PKP2):c.725C>T (p.Thr242Met) rs201580443
NM_001005242.3(PKP2):c.795G>T (p.Gly265=) rs375268778
NM_001005242.3(PKP2):c.826C>T (p.Pro276Ser) rs201944276
NM_001005242.3(PKP2):c.888C>T (p.His296=) rs397517029
NM_001005242.3(PKP2):c.909A>G (p.Glu303=)
NM_001005242.3(PKP2):c.918C>T (p.Pro306=) rs368656084
NM_001005242.3(PKP2):c.978A>G (p.Ala326=) rs775137004
NM_004572.3(PKP2):c.1104C>G (p.Ser368=) rs892666132
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.1308A>G (p.Leu436=) rs1439169005
NM_004572.3(PKP2):c.1326G>A (p.Leu442=) rs377076035
NM_004572.3(PKP2):c.1421C>T (p.Ala474Val) rs373399921
NM_004572.3(PKP2):c.1449T>C (p.Thr483=) rs781397552
NM_004572.3(PKP2):c.1476G>A (p.Thr492=) rs140301552
NM_004572.3(PKP2):c.1487T>A (p.Val496Asp) rs769899368
NM_004572.3(PKP2):c.1490G>A (p.Arg497Gln) rs781072699
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.184C>A (p.Gln62Lys) rs199601548
NM_004572.3(PKP2):c.1974A>G (p.Gln658=) rs138901574
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.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.2151G>A (p.Pro717=) rs147995773
NM_004572.3(PKP2):c.2300-4G>C rs376231586
NM_004572.3(PKP2):c.2349G>A (p.Pro783=) rs753226330
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.2490-6T>C rs761613652
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.45C>T (p.Thr15=) rs759214983
NM_004572.3(PKP2):c.486G>A (p.Thr162=) rs189040311
NM_004572.3(PKP2):c.576G>A (p.Pro192=) rs373380483
NM_004572.3(PKP2):c.600G>A (p.Val200=) rs781305034
NM_004572.3(PKP2):c.771G>A (p.Glu257=) rs1060504159
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.953A>C (p.His318Pro) rs181098323
NM_004572.3(PKP2):c.964G>T (p.Gly322Cys) rs200069860
NM_004572.3(PKP2):c.996G>A (p.Leu332=) rs144574595

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