rs945349779 Rat Genome Database

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Variant: rs945349779 -  Homo sapiens

RGD ID: 127244699
RS ID: rs945349779
ClinVar ID: CV1096935
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPL  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 19,813,601
GRCh38 8 19,956,090
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1298t1:c.1018+7T>G
NC_000008.10:g.19813601T>G
NM_000237.3:c.1018+7T>G
LRG_1298:g.59374T>G
More... 		01/25/2023 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 RCV001424145 CLINVAR
dbSNP (RS) rs945349779 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPL CLINVAR
OMIM 609708 CLINVAR