ClinVar Miner

List of variants reported as likely benign for Dilated Cardiomyopathy, Recessive

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Total variants: 56
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HGVS dbSNP
NM_000363.4(TNNI3):c.-148A>G rs73935313
NM_000363.5(TNNI3):c.-35C>A rs3729707
NM_000363.5(TNNI3):c.150+13G>A rs73617692
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.25-8T>A rs3729836
NM_001256715.2(DNAAF3):c.1001T>C (p.Leu334Pro) rs890871
NM_001256715.2(DNAAF3):c.1056G>A (p.Pro352=) rs891187
NM_001256715.2(DNAAF3):c.1093= (p.Asn365=) rs890872
NM_001256715.2(DNAAF3):c.1164-14C>T rs60176657
NM_001256715.2(DNAAF3):c.1239-8A>G rs28377509
NM_001256715.2(DNAAF3):c.1405G>A (p.Val469Met) rs114601492
NM_001256715.2(DNAAF3):c.327A>G (p.Arg109=) rs3848618
NM_001256715.2(DNAAF3):c.510A>G (p.Val170=) rs56726774
NM_001256715.2(DNAAF3):c.529G>A (p.Gly177Ser) rs58824375
NM_001256715.2(DNAAF3):c.531C>T (p.Gly177=) rs559008223
NM_001256715.2(DNAAF3):c.666T>C (p.Ala222=) rs7260320
NM_001256715.2(DNAAF3):c.790-14C>T rs7260371
NM_001256715.2(DNAAF3):c.875A>G (p.Glu292Gly) rs2365725
NM_003283.6(TNNT1):c.-20A>G rs9636153
NM_003283.6(TNNT1):c.33-8G>A rs76630067
NM_003283.6(TNNT1):c.35A>G (p.Glu12Gly) rs112562759
NM_015164.4(PLEKHM2):c.1050C>T (p.Asp350=) rs370961093
NM_015164.4(PLEKHM2):c.1065C>T (p.Asn355=) rs377142193
NM_015164.4(PLEKHM2):c.1092G>A (p.Ser364=) rs770053185
NM_015164.4(PLEKHM2):c.1110C>T (p.Ala370=) rs547428777
NM_015164.4(PLEKHM2):c.1251C>T (p.Leu417=) rs749126712
NM_015164.4(PLEKHM2):c.1418_1419delinsAT (p.Ser473Asn) rs1571067317
NM_015164.4(PLEKHM2):c.162G>A (p.Leu54=) rs199666070
NM_015164.4(PLEKHM2):c.1677C>T (p.Ser559=) rs200036096
NM_015164.4(PLEKHM2):c.1812C>T (p.Asn604=) rs370851992
NM_015164.4(PLEKHM2):c.1848C>T (p.Thr616=) rs375314550
NM_015164.4(PLEKHM2):c.1921+9C>T rs369417226
NM_015164.4(PLEKHM2):c.1956C>T (p.Ala652=) rs373293972
NM_015164.4(PLEKHM2):c.2076-4G>A rs772810642
NM_015164.4(PLEKHM2):c.2109C>T (p.Ile703=) rs1172713973
NM_015164.4(PLEKHM2):c.2209-7G>A rs528624714
NM_015164.4(PLEKHM2):c.2228G>A (p.Arg743His) rs200700186
NM_015164.4(PLEKHM2):c.2265C>T (p.Asp755=) rs370580485
NM_015164.4(PLEKHM2):c.2329A>G (p.Met777Val) rs181186746
NM_015164.4(PLEKHM2):c.2332C>T (p.Leu778=) rs370220957
NM_015164.4(PLEKHM2):c.2424G>A (p.Pro808=) rs368725345
NM_015164.4(PLEKHM2):c.2518G>A (p.Ala840Thr) rs199578594
NM_015164.4(PLEKHM2):c.2538C>T (p.Ser846=) rs372464687
NM_015164.4(PLEKHM2):c.2571C>T (p.Ser857=) rs72647153
NM_015164.4(PLEKHM2):c.2626-10C>G rs1186234870
NM_015164.4(PLEKHM2):c.2679C>T (p.Leu893=) rs1465061757
NM_015164.4(PLEKHM2):c.2700G>A (p.Thr900=) rs763833499
NM_015164.4(PLEKHM2):c.2961C>A (p.Asn987Lys) rs189025469
NM_015164.4(PLEKHM2):c.357G>C (p.Leu119=) rs201114976
NM_015164.4(PLEKHM2):c.51G>A (p.Ser17=) rs370753597
NM_015164.4(PLEKHM2):c.759C>T (p.Ser253=) rs1260718176
NM_015164.4(PLEKHM2):c.819C>T (p.Asn273=) rs374011612
NM_015164.4(PLEKHM2):c.909G>A (p.Pro303=) rs753956705
NM_015164.4(PLEKHM2):c.924G>A (p.Thr308=) rs542980745
NM_015164.4(PLEKHM2):c.981C>T (p.Ser327=) rs751424826

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