RGD:596931525 Rat Genome Database

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Variant: RGD:596931525 -  Homo sapiens

RGD ID: 596931525
ClinVar ID: CV3538733
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP2U1  LOC107986298  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 108,871,575
GRCh38 4 107,950,419
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_183075.3:c.1631G>A
NG_007961.1:g.23859G>A
NC_000004.12:g.107950419G>A
NC_000004.11:g.108871575G>A
More... 		08/19/2024 missense variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV004792859 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CYP2U1 CLINVAR
OMIM 610670 CLINVAR