RGD:150333567 Rat Genome Database

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Variant: RGD:150333567 -  Homo sapiens

RGD ID: 150333567
RS ID: rs1800168
ClinVar ID: CV1172458
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 57,592,557
GRCh38 12 57,198,774
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.11:g.57592557C>T
NM_002332.3:c.9676+104C>T
NG_016444.1:g.75276C>T
NC_000012.12:g.57198774C>T
 11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LRP1
Accession:NM_002332
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001539559 CLINVAR
dbSNP (RS) rs1800168 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRP1 CLINVAR
OMIM 107770 CLINVAR