RGD:15137767 Rat Genome Database

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Variant: RGD:15137767 -  Homo sapiens

RGD ID: 15137767
RS ID: rs1590141783
ClinVar ID: CV787712
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPL  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 19,809,469
GRCh38 8 19,951,958
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000237.3:c.429+10G>A
NG_008855.2:g.55242G>A
NC_000008.11:g.19951958G>A
NC_000008.10:g.19809469G>A
More... 		12/19/2018 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 RCV000982359 CLINVAR
dbSNP (RS) rs1590141783 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPL CLINVAR
OMIM 609708 CLINVAR