ClinVar Miner

List of variants reported as benign for arrhythmogenic right ventricular dysplasia 13 by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (1):
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Minimum conflict level:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_013266.4(CTNNA3):c.1281+18601C>T rs6480209 0.48391
NM_013266.4(CTNNA3):c.1787G>A (p.Ser596Asn) rs4548513 0.47526
NM_013266.4(CTNNA3):c.292+13A>G rs3750863 0.45524
NM_013266.4(CTNNA3):c.2266-10T>G rs2105702 0.32828
NM_013266.4(CTNNA3):c.293-19A>T rs1909654 0.20576
NM_013266.4(CTNNA3):c.579+15T>G rs10997691 0.12289
NM_013266.4(CTNNA3):c.460-13T>C rs7903421 0.05538
NM_013266.4(CTNNA3):c.1872C>A (p.Val624=) rs10997034 0.04630
NM_013266.4(CTNNA3):c.1531+16T>C rs78806593 0.03870
NM_013266.4(CTNNA3):c.843+17A>G rs77409659 0.02787
NM_013266.4(CTNNA3):c.1655C>T (p.Thr552Met) rs61737718 0.02389
NM_013266.4(CTNNA3):c.393G>A (p.Ala131=) rs80182543 0.02215
NM_013266.4(CTNNA3):c.478T>A (p.Ser160Thr) rs61749223 0.01916
NM_013266.4(CTNNA3):c.348A>C (p.Pro116=) rs61749224 0.01511
NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys) rs41274090 0.01060
NM_013266.4(CTNNA3):c.1047C>T (p.Asn349=) rs60262757 0.00761
NM_013266.4(CTNNA3):c.2553G>A (p.Lys851=) rs115814032 0.00420
NM_013266.4(CTNNA3):c.99+11C>T rs115451937 0.00411
NM_013266.4(CTNNA3):c.2142G>A (p.Glu714=) rs115972723 0.00315
NM_013266.4(CTNNA3):c.1587T>A (p.Asp529Glu) rs74141466 0.00293
NM_013266.4(CTNNA3):c.1588G>T (p.Ala530Ser) rs74141465 0.00293
NM_013266.4(CTNNA3):c.1611G>A (p.Ala537=) rs146900023 0.00266
NM_013266.4(CTNNA3):c.483C>T (p.Leu161=) rs74142830 0.00255
NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His) rs143682596 0.00240
NM_013266.4(CTNNA3):c.33C>T (p.Ile11=) rs61735044 0.00206
NM_013266.4(CTNNA3):c.2172A>C (p.Pro724=) rs116662854 0.00191
NM_013266.4(CTNNA3):c.742G>T (p.Ala248Ser) rs192093851 0.00189
NM_013266.4(CTNNA3):c.1195C>A (p.Leu399Ile) rs115276158 0.00178
NM_013266.4(CTNNA3):c.429T>C (p.Asp143=) rs111880127 0.00178
NM_013266.4(CTNNA3):c.580-8C>T rs141983252 0.00170
NM_013266.4(CTNNA3):c.2158A>C (p.Arg720=) rs143867269 0.00169
NM_013266.4(CTNNA3):c.844-15G>A rs201089736 0.00098
NM_013266.4(CTNNA3):c.2160-19T>C rs200450770 0.00086
NM_013266.4(CTNNA3):c.156G>C (p.Ser52=) rs61759502 0.00064
NM_013266.4(CTNNA3):c.1929C>T (p.His643=) rs147760277 0.00055
NM_013266.4(CTNNA3):c.2159+15A>G rs749117441 0.00034
NM_013266.4(CTNNA3):c.387G>A (p.Leu129=) rs143943926 0.00026
NM_013266.4(CTNNA3):c.1422G>A (p.Ala474=) rs372258059 0.00022
NM_013266.4(CTNNA3):c.2601G>A (p.Thr867=) rs575703238 0.00022
NM_013266.4(CTNNA3):c.779A>G (p.Gln260Arg) rs190073606 0.00022
NM_013266.4(CTNNA3):c.1977+18G>C rs574293198 0.00014
NM_013266.4(CTNNA3):c.1978-9A>G rs771655401 0.00009
NM_013266.4(CTNNA3):c.399G>A (p.Thr133=) rs150376558 0.00009
NM_013266.4(CTNNA3):c.1959C>T (p.Thr653=) rs556623128 0.00006
NM_013266.4(CTNNA3):c.1215T>C (p.Asn405=) rs775938724 0.00004
NM_013266.4(CTNNA3):c.2401-11T>G rs761888151 0.00004
NM_013266.4(CTNNA3):c.2133C>T (p.Ile711=) rs754084649 0.00002
NM_013266.4(CTNNA3):c.1318G>A (p.Asp440Asn) rs545174357 0.00001
NM_013266.4(CTNNA3):c.1048-12dup
NM_013266.4(CTNNA3):c.1587_1588delinsAT (p.Asp529_Ala530delinsGluSer) rs1554949356
NM_013266.4(CTNNA3):c.2401-23dup rs1338241471
NM_013266.4(CTNNA3):c.240T>C (p.Ala80=)

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