RGD:28873873 Rat Genome Database

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Variant: RGD:28873873 -  Homo sapiens

RGD ID: 28873873
RS ID: rs920755267
ClinVar ID: CV891758
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 15,603,192
GRCh38 4 15,601,569
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_697t1:c.*144A>C
NM_001080522.2:c.*144A>C
LRG_697:g.136704A>C
NG_013035.1:g.136704A>C
More... 		01/13/2018 downstream transcript variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001146956 CLINVAR
  RCV001146957 CLINVAR
dbSNP (RS) rs920755267 CLINVAR
MedGen C2676788 CLINVAR
  C2676790 CLINVAR
NCBI Gene CC2D2A CLINVAR
OMIM 612013 CLINVAR
  612284 CLINVAR
  612285 CLINVAR