RGD:152105996 Rat Genome Database

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Variant: RGD:152105996 -  Homo sapiens

RGD ID: 152105996
RS ID: rs377174833
ClinVar ID: CV1609574
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SORL1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 121,489,618
GRCh38 11 121,618,909
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003105.6:c.5724+16C>T
NG_023313.1:g.171658C>T
NC_000011.10:g.121618909C>T
NC_000011.9:g.121489618C>T
 12/13/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SORL1
Accession:NM_003105
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002115940 CLINVAR
dbSNP (RS) rs377174833 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SORL1 CLINVAR
OMIM 602005 CLINVAR