rs491785 Rat Genome Database

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Variant: rs491785 -  Homo sapiens

RGD ID: 150457811
RS ID: rs491785
ClinVar ID: CV1237127
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 108,724,693
GRCh38 1 108,182,071
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_213651.3:c.254-43C>T
NM_013386.5:c.311-43C>T
NG_032752.1:g.23288C>T
NC_000001.11:g.108182071G>A
More...
05/14/2021 intron variant benign none provided

Gene Symbol:SLC25A24
Accession:NM_013386
Location:INTRON

Gene Symbol:SLC25A24
Accession:NM_213651
Location:INTRON

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PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001648806 CLINVAR
dbSNP (RS) rs491785 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR