rs34563977 Rat Genome Database

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Variant: rs34563977 -  Homo sapiens

RGD ID: 150491907
RS ID: rs34563977
ClinVar ID: CV1267853
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 108,681,600
GRCh38 1 108,138,978
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_032752.1:g.66381A>G
NC_000001.11:g.108138978T>C
NC_000001.10:g.108681600T>C
NM_213651.3:c.1192+80A>G
More... 		05/16/2021 intron variant benign none provided

Gene Symbol:SLC25A24
Accession:NM_013386
Location:INTRON

Gene Symbol:SLC25A24
Accession:NM_213651
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001687878 CLINVAR
dbSNP (RS) rs34563977 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR