rs7173941 Rat Genome Database

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Variant: rs7173941 -  Homo sapiens

RGD ID: 150482608
RS ID: rs7173941
ClinVar ID: CV1244303
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ETFA  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 76,588,322
GRCh38 15 76,295,981
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001127716.2:c.40-3281C>T
NM_000126.4:c.40-244C>T
NC_000015.9:g.76588322G>A
NG_007077.2:g.20489C>T
More... 		07/21/2018 intron variant 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 RCV001653150 CLINVAR
dbSNP (RS) rs7173941 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ETFA CLINVAR
OMIM 608053 CLINVAR