rs189781826 Rat Genome Database

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Variant: rs189781826 -  Homo sapiens

RGD ID: 11594153
RS ID: rs189781826
ClinVar ID: CV279719
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 236,646,366
GRCh38 1 236,483,066
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011566.1:g.93687G>A
NC_000001.11:g.236483066G>A
NC_000001.10:g.236646366G>A
NG_001115.8:g.69G>A
More... 		01/13/2018 3 prime utr variant benign|uncertain significance
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:EDARADD
Accession:NM_145861
Location:3UTRS;EXON

Gene Symbol:EDARADD
Accession:NM_080738
Location:3UTRS;EXON

Gene Symbol:EDARADD
Accession:NM_001422628
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000356260 CLINVAR
  RCV001097004 CLINVAR
dbSNP (RS) rs189781826 CLINVAR
MedGen C5848103 CLINVAR
  CN239465 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR
  614941 CLINVAR