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Variant : CV403364 (NC_000019.9:g.(?_11223954)_(11244506_?)del) Homo sapiens

Symbol: CV403364
Name: NC_000019.9:g.(?_11223954)_(11244506_?)del
Condition: Familial hypercholesterolemia [RCV000469198]
Clinical Significance: pathogenic
Last Evaluated: 08/06/2016
Review Status: criteria provided, single submitter
Related Genes: LDLR   MIR6886  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000019.9:g.(?_11223954)_(11244506_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381911,113,278 - 11,133,830CLINVAR
GRCh371911,223,954 - 11,244,506CLINVAR
Cytogenetic Map1919p13.2CLINVAR
Trait Synonyms: Fredrickson type IIa hyperlipoproteinemia; HYPER-LOW-DENSITY-LIPOPROTEINEMIA; HYPERCHOLESTEROLEMIA, FAMILIAL, 1; HYPERCHOLESTEROLEMIA, FAMILIAL, MODIFIER OF; HYPERCHOLESTEROLEMIC XANTHOMATOSIS, FAMILIAL; Hyperlipoproteinemia Type II; Hyperlipoproteinemia Type IIa; LDL RECEPTOR DISORDER
Prevalence: 1-9 / 1 000 000



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12887511
Created: 2017-05-09
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.