RGD:11620622 Rat Genome Database

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Variant: RGD:11620622 -  Homo sapiens

RGD ID: 11620622
RS ID: rs879386992
ClinVar ID: CV327250
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 64,358,473
GRCh38 11 64,591,001
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008110.1:g.5192G>A
NC_000011.10:g.64591001G>A
NC_000011.9:g.64358473G>A
NM_001276327.1:c.-556G>A
More... 		06/14/2016 5 prime utr variant uncertain significance Renal hypouricemia
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000338930 CLINVAR
dbSNP (RS) rs879386992 CLINVAR
MedGen C0473219 CLINVAR
NCBI Gene SLC22A12 CLINVAR
OMIM 220150 CLINVAR
  607096 CLINVAR
SNOMED CT 236478009 CLINVAR