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Variant : CV228147 (NM_000527.4(LDLR):c.796G>A (p.Asp266Asn)) Homo sapiens

Symbol: CV228147
Name: NM_000527.4(LDLR):c.796G>A (p.Asp266Asn)
Condition: Familial hypercholesterolemia [RCV000211615]
Clinical Significance: pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
Last Evaluated: 09/19/2017
Review Status: criteria provided, conflicting interpretations|criteria provided, multiple submitters, no conflicts|no assertion criteria provided
Related Genes: LDLR  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): LRG_274t1:c.796G>A
NM_000527.4:c.796G>A
LRG_274:g.22286G>A
NG_009060.1:g.22286G>A
NC_000019.10:g.11106666G>A
NC_000019.9:g.11217342G>A
LRG_274p1:p.Asp266Asn
NP_000518.1:p.Asp266Asn
c.796G>A
NM_001195803.2:c.415G>A
NM_001195799.2:c.673G>A
NM_000527.4:c.796G>A
NM_001195798.2:c.796G>A
NP_001182732.1:p.Asp139Asn
NP_001182728.1:p.Asp225Asn
NM_001195800.2:c.314-726G>A
NP_001182727.1:p.Asp266Asn
Position
Human AssemblyChrPosition (strand)Source
GRCh381911,106,666 - 11,106,666CLINVAR
GRCh371911,217,342 - 11,217,342CLINVAR
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 - curated
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11088002
Created: 2016-06-07
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.