RGD:150510740 Rat Genome Database

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Variant: RGD:150510740 -  Homo sapiens

RGD ID: 150510740
RS ID: rs34810921
ClinVar ID: CV1242489
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 57,531,951
GRCh38 12 57,138,168
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002332.3:c.68-291C>T
NG_016444.1:g.14670C>T
NC_000012.12:g.57138168C>T
NC_000012.11:g.57531951C>T
 06/20/2021 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 RCV001660840 CLINVAR
dbSNP (RS) rs34810921 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRP1 CLINVAR
OMIM 107770 CLINVAR