RGD:11593006 Rat Genome Database

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Variant: RGD:11593006 -  Homo sapiens

RGD ID: 11593006
RS ID: rs34993359
ClinVar ID: CV299297
Genic Status: INTERGENIC
Type: deletion (SO:0000159) 
Reference Nucleotide: A
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 4 68,621,586
GRCh38 4 67,755,868
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009293.1:g.5219del
NC_000004.12:g.67755877del
NC_000004.11:g.68621595del
NM_000406.2:c.-1533delT
More...
06/26/2018 5 prime utr variant benign|likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000344654 CLINVAR
  RCV001683391 CLINVAR
dbSNP (RS) rs34993359 CLINVAR
MedGen C3661900 CLINVAR
  CN239347 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR