RGD:11656508 Rat Genome Database

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Variant: RGD:11656508 -  Homo sapiens

RGD ID: 11656508
RS ID: rs886057415
ClinVar ID: CV351415
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127895927  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 32,870,790
GRCh38 22 32,474,803
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000022.11:g.32474803G>A
NC_000022.10:g.32870790G>A
NG_016001.2:g.5084G>A
NM_012179.3:c.-200G>A
More... 		06/14/2016 2kb upstream variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000334060 CLINVAR
dbSNP (RS) rs886057415 CLINVAR
MedGen CN239372 CLINVAR
NCBI Gene FBXO7 CLINVAR
OMIM 605648 CLINVAR