RGD:405245335 Rat Genome Database

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Variant: RGD:405245335 -  Homo sapiens

RGD ID: 405245335
ClinVar ID: CV3051458
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LIPG  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 18 47,110,084
GRCh38 18 49,583,714
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001308006.2:c.1094A>G
NM_006033.4:c.1316A>G
NC_000018.10:g.49583714A>G
NC_000018.9:g.47110084A>G
More... 		01/18/2024 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003720266 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LIPG CLINVAR
OMIM 603684 CLINVAR