rs367977687 Rat Genome Database

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Variant: rs367977687 -  Homo sapiens

RGD ID: 11665793
RS ID: rs367977687
ClinVar ID: CV353158
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACTA2-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 90,694,822
GRCh38 10 88,935,065
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_781:g.61326G>A
NG_011541.1:g.61326G>A
NC_000010.11:g.88935065C>T
NC_000010.10:g.90694822C>T
More... 		06/14/2016 500b downstream variant|non-coding transcript variant likely benign infancy <1 / 1 000 000 Moyamoya syndrome; MYDRIASIS, CONGENITAL, WITH PATENT DUCTUS ARTERIOSUS, THORACIC AORTIC ANEURYSM, AND VASCULOPATHY; none provided; Thoracic aortic aneurysms and dissections
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ACTA2-AS1
Accession:NR_125373
Location:EXON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000294662 CLINVAR
  RCV000326308 CLINVAR
  RCV000389043 CLINVAR
  RCV004705500 CLINVAR
dbSNP (RS) rs367977687 CLINVAR
MedGen C0026654 CLINVAR
  C3151201 CLINVAR
  C3661900 CLINVAR
  C4707243 CLINVAR
NCBI Gene ACTA2 CLINVAR
  ACTA2-AS1 CLINVAR
OMIM 102620 CLINVAR
  252350 CLINVAR
  613834 CLINVAR
SNOMED CT 69116000 CLINVAR