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| Dilated Cardiomyopathy and conduction defects v1.55 | SGCD | Rebecca Whittington commented on gene: SGCD: Cardiomyopathy, dilated, 1L OMIM#606685; Muscular dystrophy, limb-girdle, autosomal recessive 6 OMIM#601287 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.54 | SGCD | Rebecca Whittington commented on gene: SGCD: HGMD: 6 variants all but one ?DM, though a number listed in Walsh through LMM and classified as LP. Included in review of DCM genes: Dalin 2017 International Journal of Cardiology 228 (2017) 742748 (no variants though), Hershberger 2013 Nat Rev Cardiol 10:531. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.53 | SGCD | Rebecca Whittington reviewed gene: SGCD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.47 | SGCD |
Ellen McDonagh Source South West GLH was added to SGCD. Mode of inheritance for gene SGCD was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
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| Dilated Cardiomyopathy and conduction defects v1.46 | SGCD | Ellen McDonagh reviewed gene: SGCD: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.45 | SGCD | Ellen McDonagh Source London South GLH was added to SGCD. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.44 | SGCD | James Eden reviewed gene: SGCD: Rating: RED; Mode of pathogenicity: ; Publications: 19259135, 20186049, 27532257; Phenotypes: Cardiomyopathy, dilated, 1L (606685), Muscular dystrophy, limb-girdle, autosomal recessive 6 (601287); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.43 | SGCD |
Ellen McDonagh Source North West GLH was added to SGCD. Added phenotypes Muscular dystrophy, limb-girdle, autosomal recessive 6 (601287); Cardiomyopathy, dilated, 1L (606685) for gene: SGCD Publications for gene SGCD were changed from to 27532257; 20186049; 19259135 |
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| Dilated Cardiomyopathy and conduction defects v1.40 | SGCD | Oxford Medical Genetics Laboratory commented on gene: SGCD: Not fully reviewed. Would be interested to hear findings of Manchester laboratory testing this gene in DCM cohorts. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy and conduction defects v1.39 | SGCD |
Ellen McDonagh Source Wessex and West Midlands GLH was added to SGCD. Rating Changed from Green List (high evidence) to Green List (high evidence) |
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