RGD:11609857 Rat Genome Database

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Variant: RGD:11609857 -  Homo sapiens

RGD ID: 11609857
RS ID: rs9734313
ClinVar ID: CV321162
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 64,358,311
GRCh38 11 64,590,839
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.5030C>T
NC_000011.10:g.64590839C>T
NC_000011.9:g.64358311C>T
NM_144585.3:c.-718C>T
More...
11/12/2018 5 prime utr variant benign none provided; Renal hypouricemia
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000373468 CLINVAR
  RCV001642950 CLINVAR
dbSNP (RS) rs9734313 CLINVAR
MedGen C0473219 CLINVAR
  C3661900 CLINVAR
NCBI Gene SLC22A12 CLINVAR
OMIM 220150 CLINVAR
  607096 CLINVAR
SNOMED CT 236478009 CLINVAR