rs1459602794 Rat Genome Database

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Variant: rs1459602794 -  Homo sapiens

RGD ID: 28891050
RS ID: rs1459602794
ClinVar ID: CV893857
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129993734  RETREG1-AS1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 16,617,142
GRCh38 5 16,617,033
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_363t1:c.-62C>A
NC_000005.10:g.16617033G>T
NC_000005.9:g.16617142G>T
NG_016644.2:g.4977C>A
More... 		01/13/2018 5 prime utr variant uncertain significance Hereditary sensory and autonomic neuropathy type IIB
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RETREG1-AS1
Accession:NR_109946
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001152642 CLINVAR
dbSNP (RS) rs1459602794 CLINVAR
MedGen C2751092 CLINVAR
NCBI Gene 101929524 CLINVAR
  LOC129993734 CLINVAR
  RETREG1 CLINVAR
OMIM 613114 CLINVAR
  613115 CLINVAR