RGD:34893092 Rat Genome Database

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Variant: RGD:34893092 -  Homo sapiens

RGD ID: 34893092
RS ID: rs17249141
ClinVar ID: CV914649
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LDLR-AS1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 11,200,008
GRCh38 19 11,089,332
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_274:g.4952C>G
NG_009060.1:g.4952C>G
NC_000019.10:g.11089332C>G
NC_000019.9:g.11200008C>G
More... 		08/27/2023 non-coding transcript variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LDLR-AS1
Accession:NR_163945
Location:EXON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001183583 CLINVAR
dbSNP (RS) rs17249141 CLINVAR
MedGen C0020445 CLINVAR
NCBI Gene LDLR CLINVAR
  LDLR-AS1 CLINVAR
OMIM 606945 CLINVAR
SNOMED CT 398036000 CLINVAR