rs6856745 Rat Genome Database

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Variant: rs6856745 -  Homo sapiens

RGD ID: 152026242
RS ID: rs6856745
ClinVar ID: CV1540697
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP2U1  LOC107986298  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 108,868,515
GRCh38 4 107,947,359
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000004.12:g.107947359T>A
NC_000004.11:g.108868515T>A
NM_183075.3:c.1127-17T>A
NG_007961.1:g.20799T>A
 06/03/2021 intron variant likely benign
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1540697Humanparaplegia  IAGP 8554872ClinVar Annotator: match by term: Spastic paraplegiaClinVarPMID:28492532

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1540697HumanSpastic paraplegia  IAGP 8554872ClinVar Annotator: match by term: Spastic paraplegiaClinVarPMID:28492532
Gene Symbol:CYP2U1
Accession:NM_183075
Location:INTRON

Gene Symbol:CYP2U1
Accession:XM_005262717
Location:INTRON

Gene Symbol:CYP2U1
Accession:XM_005262720
Location:INTRON

Gene Symbol:LOC107986298
Accession:XR_001741784
Location:INTRON;NON-CODING

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002104490 CLINVAR
dbSNP (RS) rs6856745 CLINVAR
MedGen C0037772 CLINVAR
NCBI Gene CYP2U1 CLINVAR
OMIM 610670 CLINVAR