RGD:405222904 Rat Genome Database

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Variant: RGD:405222904 -  Homo sapiens

RGD ID: 405222904
ClinVar ID: CV2908544
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPL  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 19,822,807
GRCh38 8 19,965,296
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1298t1:c.1428-14G>C
NM_000237.3:c.1428-14G>C
LRG_1298:g.68580G>C
NG_008855.2:g.68580G>C
More... 		08/04/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LPL
Accession:NM_000237
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003568705 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPL CLINVAR
OMIM 609708 CLINVAR