Knowledge base for genomic medicine in Japanese
家族性高コレステロール血症
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
Duplicationc.(190+1_191-1)_(940+1_941-1)dupLDLRLikely pathogenic191121102211221327nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000030
Deletionc.(190+1_191-1)_(1060+1_1061-1)delLDLRPathogenic191121102211222189nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000033
Duplicationc.(190+1_191-1)_(1186+1_1187-1)dupLDLRLikely pathogenic191121102211223953nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000427
Deletionc.(190+1_191-1)_(1586+1_1587-1)delLDLRPathogenic191121102211226769nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_001289
Deletionc.(190+1_191-1)_(1845+1_1846-1)delLDLRPathogenic191121102211230767nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000032
Duplicationc.(190+1_191-1)_(1845+1_1846-1)dupLDLRPathogenic191121102211230767nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_001297
Duplicationc.(190+1_191-1)_(2140+1_2141-1)dupLDLRLikely pathogenic191121102211233849nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000434
Deletionc.(313+1_314-1)_(694+1_695-1)delLDLRPathogenic191121346311217240nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_001008
Duplicationc.(313+1_314-1)_(817+1_818-1)dupLDLRLikely pathogenic191121346311218067nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_000777
Duplicationc.(313+1_314-1)_(940+1_941-1)dupLDLRLikely pathogenic191121346311221327nanacriteria provided, single submitterLDLR-LOVD, British Heart Foundation:LDLR_001300