RGD:405182221 Rat Genome Database

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Variant: RGD:405182221 -  Homo sapiens

RGD ID: 405182221
ClinVar ID: CV3147624
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LIPG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 18 47,101,932
GRCh38 18 49,575,562
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.572-5853C>T
NM_006033.4:c.765C>T
NC_000018.10:g.49575562C>T
NC_000018.9:g.47101932C>T
More... 		01/25/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003842526 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LIPG CLINVAR
OMIM 603684 CLINVAR