rs184053874 Rat Genome Database

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Variant: rs184053874 -  Homo sapiens

RGD ID: 150331845
RS ID: rs184053874
ClinVar ID: CV1169650
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ETFA  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 76,524,040
GRCh38 15 76,231,699
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000015.10:g.76231699A>G
NC_000015.9:g.76524040A>G
NM_001127716.2:c.670-301T>C
NG_007077.2:g.84771T>C
More... 		06/28/2018 intron variant likely benign none provided

Gene Symbol:ETFA
Accession:NM_001127716
Location:INTRON

Gene Symbol:ETFA
Accession:NM_000126
Location:INTRON

Gene Symbol:ETFA
Accession:XR_007064434
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV001536649 CLINVAR
dbSNP (RS) rs184053874 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ETFA CLINVAR
OMIM 608053 CLINVAR