Duplication | NM_000527.5(LDLR):c.41dup (p.Leu14fs) | LDLR | Pathogenic | 19 | 11200265 | 11200265 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584730,LDLR-LOVD, British Heart Foundation:LDLR_001132 |
Deletion | NM_000527.5(LDLR):c.41del (p.Leu14fs) | LDLR | Pathogenic | 19 | 11200264 | 11200264 | CT | C | criteria provided, single submitter | ClinGen:CA10584729,LDLR-LOVD, British Heart Foundation:LDLR_000011 |
Deletion | NM_000527.5(LDLR):c.28_38del (p.Trp10fs) | LDLR | Pathogenic | 19 | 11200252 | 11200262 | GCGCTGGACCGT | G | criteria provided, single submitter | ClinGen:CA10584727,LDLR-LOVD, British Heart Foundation:LDLR_001677 |
Duplication | NM_000527.5(LDLR):c.33_36dup (p.Ala13fs) | LDLR | Pathogenic | 19 | 11200257 | 11200260 | A | ACCGT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584728,LDLR-LOVD, British Heart Foundation:LDLR_001703 |
single nucleotide variant | NM_000527.5(LDLR):c.30G>A (p.Trp10Ter) | LDLR | Pathogenic | 19 | 11200254 | 11200254 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000527.5(LDLR):c.28T>C (p.Trp10Arg) | LDLR | Pathogenic/Likely pathogenic | 19 | 11200252 | 11200252 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584726,LDLR-LOVD, British Heart Foundation:LDLR_000260 |
single nucleotide variant | NM_000527.5(LDLR):c.28T>A (p.Trp10Arg) | LDLR | Likely pathogenic | 19 | 11200252 | 11200252 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584725,LDLR-LOVD, British Heart Foundation:LDLR_001681 |
Insertion | NM_000527.5(LDLR):c.16_17insTTCCT (p.Trp6fs) | LDLR | Likely pathogenic | 19 | 11200238 | 11200239 | G | GCTTTC | criteria provided, single submitter | ClinGen:CA085175 |
single nucleotide variant | NM_000527.5(LDLR):c.12G>A (p.Trp4Ter) | LDLR | Pathogenic | 19 | 11200236 | 11200236 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA085131,LDLR-LOVD, British Heart Foundation:LDLR_000357 |
single nucleotide variant | NM_000527.5(LDLR):c.11G>A (p.Trp4Ter) | LDLR | Pathogenic | 19 | 11200235 | 11200235 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584724,LDLR-LOVD, British Heart Foundation:LDLR_001492 |