RGD:13525592 Rat Genome Database

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Variant: RGD:13525592 -  Homo sapiens

RGD ID: 13525592
RS ID: rs1554620947
ClinVar ID: CV503101
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VLDLR  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 2,643,150
GRCh38 9 2,643,150
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.2643150C>G
NC_000009.11:g.2643150C>G
NM_003383.3:c.449-10C>G
NM_001322225.2:c.326-10C>G
More... 		09/29/2017 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:VLDLR
Accession:NM_001322226
Location:INTRON

Gene Symbol:VLDLR
Accession:NM_001322225
Location:INTRON

Gene Symbol:VLDLR
Accession:NM_001018056
Location:INTRON

Gene Symbol:VLDLR
Accession:NM_003383
Location:INTRON

Gene Symbol:VLDLR
Accession:XM_047423848
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000603294 CLINVAR
dbSNP (RS) rs1554620947 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene VLDLR CLINVAR
OMIM 192977 CLINVAR