RGD:11659172 Rat Genome Database

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Variant: RGD:11659172 -  Homo sapiens

RGD ID: 11659172
RS ID: rs886057400
ClinVar ID: CV337856
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 32,439,246
GRCh38 22 32,043,259
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
NG_017045.1:g.5228G>A
NC_000022.11:g.32043259G>A
NC_000022.10:g.32439246G>A
NM_000343.3:c.-23G>A
 06/14/2016 5 prime utr variant uncertain significance infancy Carbohydrate intolerance of glucose galactose; Complex carbohydrate intolerance; Glucose galactose malabsorption deficiency; Monosaccharide malabsorption
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355450 CLINVAR
dbSNP (RS) rs886057400 CLINVAR
MedGen C0268186 CLINVAR
NCBI Gene SLC5A1 CLINVAR
OMIM 182380 CLINVAR
  606824 CLINVAR
SNOMED CT 27943000 CLINVAR