rs61740489 Rat Genome Database

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Variant: rs61740489 -  Homo sapiens

RGD ID: 28892394
RS ID: rs61740489
ClinVar ID: CV863975
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  ENO1P1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 236,646,915
GRCh38 1 236,483,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000001.10:g.236646915A>G
NM_145861.2:c.*966A>G
NG_011566.1:g.94236A>G
NC_000001.11:g.236483615A>G
More... 		01/13/2018 3 prime utr variant benign none provided
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV863975Humanhypohidrotic ectodermal dysplasia  IAGP 8554872ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasiaClinVarPMID:25741868

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV863975HumanHypohidrotic ectodermal dysplasia  IAGP 8554872ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasiaClinVarPMID:25741868
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

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001100552 CLINVAR
  RCV004714183 CLINVAR
dbSNP (RS) rs61740489 CLINVAR
MedGen C3661900 CLINVAR
  C5848103 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR
  614941 CLINVAR