ClinVar Miner

List of variants reported as likely benign for Primary dilated cardiomyopathy; Hypertrophic cardiomyopathy

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ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_014476.6(PDLIM3):c.715G>A (p.Asp239Asn) rs142143310 0.00046
NM_014476.6(PDLIM3):c.169A>G (p.Thr57Ala) rs142951316 0.00031
NM_014476.6(PDLIM3):c.963C>T (p.Ala321=) rs148518020 0.00029
NM_014476.6(PDLIM3):c.1053C>T (p.Pro351=) rs369891118 0.00019
NM_014476.6(PDLIM3):c.663-15G>A rs561379714 0.00017
NM_014476.6(PDLIM3):c.399-18G>A rs372273108 0.00016
NM_014476.6(PDLIM3):c.697G>C (p.Val233Leu) rs143121072 0.00016
NM_014476.6(PDLIM3):c.696C>T (p.Asp232=) rs148256486 0.00013
NM_014476.6(PDLIM3):c.399-19C>T rs201237568 0.00008
NM_014476.6(PDLIM3):c.375T>C (p.Pro125=) rs372840074 0.00006
NM_014476.6(PDLIM3):c.54A>G (p.Ser18=) rs768654855 0.00006
NM_014476.6(PDLIM3):c.240T>C (p.Ile80=) rs376278294 0.00005
NM_014476.6(PDLIM3):c.1032C>T (p.His344=) rs200734614 0.00004
NM_014476.6(PDLIM3):c.168G>A (p.Gly56=) rs151119100 0.00004
NM_014476.6(PDLIM3):c.693G>A (p.Ser231=) rs756066114 0.00004
NM_014476.6(PDLIM3):c.858C>T (p.Gly286=) rs151318437 0.00004
NM_014476.6(PDLIM3):c.906-17G>A rs199828661 0.00004
NM_014476.6(PDLIM3):c.417C>T (p.Ser139=) rs200230349 0.00003
NM_014476.6(PDLIM3):c.114G>A (p.Ala38=) rs377383830 0.00002
NM_014476.6(PDLIM3):c.330+7G>A rs369445862 0.00002
NM_014476.6(PDLIM3):c.501G>A (p.Ala167=) rs142771915 0.00002
NM_014476.6(PDLIM3):c.588G>A (p.Leu196=) rs760087085 0.00002
NM_014476.6(PDLIM3):c.861G>A (p.Gly287=) rs764585438 0.00002
NM_014476.6(PDLIM3):c.1071G>A (p.Thr357=) rs772388695 0.00001
NM_014476.6(PDLIM3):c.159C>T (p.Asp53=) rs781147581 0.00001
NM_014476.6(PDLIM3):c.258C>T (p.His86=) rs1189554604 0.00001
NM_014476.6(PDLIM3):c.398+9C>T rs761820729 0.00001
NM_014476.6(PDLIM3):c.408C>T (p.Ser136=) rs764271627 0.00001
NM_014476.6(PDLIM3):c.567G>A (p.Gln189=) rs776361335 0.00001
NM_014476.6(PDLIM3):c.662+7T>C rs1580239101 0.00001
NM_014476.6(PDLIM3):c.66C>T (p.Asp22=) rs770008147 0.00001
NM_014476.6(PDLIM3):c.687C>T (p.Pro229=) rs753543916 0.00001
NM_014476.6(PDLIM3):c.711C>G (p.Leu237=) rs1280400272 0.00001
NM_014476.6(PDLIM3):c.783C>T (p.Asp261=) rs201775052 0.00001
NM_014476.6(PDLIM3):c.879C>T (p.Leu293=) rs766386102 0.00001
NM_014476.6(PDLIM3):c.894G>C (p.Gly298=) rs951740054 0.00001
NM_014476.6(PDLIM3):c.905+10A>G rs1250327271 0.00001
NM_014476.6(PDLIM3):c.924G>A (p.Ala308=) rs558471910 0.00001
NM_014476.6(PDLIM3):c.1027A>G (p.Thr343Ala) rs569673500
NM_014476.6(PDLIM3):c.1035A>G (p.Ala345=)
NM_014476.6(PDLIM3):c.1078C>T (p.Leu360=) rs974220815
NM_014476.6(PDLIM3):c.138A>C (p.Gly46=)
NM_014476.6(PDLIM3):c.195G>T (p.Ala65=)
NM_014476.6(PDLIM3):c.246-19A>G
NM_014476.6(PDLIM3):c.246-9T>C rs2153337858
NM_014476.6(PDLIM3):c.261A>G (p.Leu87=) rs2153337849
NM_014476.6(PDLIM3):c.331-15G>A
NM_014476.6(PDLIM3):c.398+12T>A
NM_014476.6(PDLIM3):c.398+12T>C
NM_014476.6(PDLIM3):c.398+15G>A rs1259024974
NM_014476.6(PDLIM3):c.398+8G>A rs1215013585
NM_014476.6(PDLIM3):c.399-17dup rs1176465439
NM_014476.6(PDLIM3):c.399-9T>C rs2153333102
NM_014476.6(PDLIM3):c.417C>A (p.Ser139=) rs200230349
NM_014476.6(PDLIM3):c.465T>C (p.Thr155=) rs2095701642
NM_014476.6(PDLIM3):c.474C>T (p.Thr158=)
NM_014476.6(PDLIM3):c.537A>G (p.Glu179=) rs750215417
NM_014476.6(PDLIM3):c.558A>G (p.Val186=) rs2153332982
NM_014476.6(PDLIM3):c.579T>C (p.Pro193=)
NM_014476.6(PDLIM3):c.594A>G (p.Ser198=)
NM_014476.6(PDLIM3):c.663-18G>A
NM_014476.6(PDLIM3):c.663-19C>T
NM_014476.6(PDLIM3):c.672A>T (p.Thr224=)
NM_014476.6(PDLIM3):c.750G>A (p.Ser250=)
NM_014476.6(PDLIM3):c.780G>A (p.Val260=) rs2153332313
NM_014476.6(PDLIM3):c.794-14G>C
NM_014476.6(PDLIM3):c.794-15C>T
NM_014476.6(PDLIM3):c.804G>A (p.Pro268=)
NM_014476.6(PDLIM3):c.822G>A (p.Val274=) rs1580233408
NM_014476.6(PDLIM3):c.834G>A (p.Val278=)
NM_014476.6(PDLIM3):c.837G>A (p.Thr279=) rs199895839
NM_014476.6(PDLIM3):c.837G>C (p.Thr279=)
NM_014476.6(PDLIM3):c.861G>T (p.Gly287=) rs764585438
NM_014476.6(PDLIM3):c.906-8C>T
NM_014476.6(PDLIM3):c.93+13A>C
NM_014476.6(PDLIM3):c.93+16C>A rs557718466
NM_014476.6(PDLIM3):c.93+9C>A rs961788900
NM_014476.6(PDLIM3):c.93+9C>G
NM_014476.6(PDLIM3):c.94-11A>T
NM_014476.6(PDLIM3):c.94-14A>G
NM_014476.6(PDLIM3):c.94-7C>A
NM_014476.6(PDLIM3):c.954C>T (p.Phe318=) rs757507673
NM_014476.6(PDLIM3):c.975C>T (p.Leu325=)

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