rs279558 Rat Genome Database

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Variant: rs279558 -  Homo sapiens

RGD ID: 150500216
RS ID: rs279558
ClinVar ID: CV1212169
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: JAGN1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 9,932,337
GRCh38 3 9,890,653
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1228t1:c.-70G>C
NM_001363890.1:c.-338G>C
NM_032492.4:c.-70G>C
LRG_1228:g.5067G>C
More... 		05/12/2021 5 prime utr variant benign none provided

Gene Symbol:JAGN1
Accession:NM_032492
Location:5UTRS;EXON

Gene Symbol:JAGN1
Accession:NM_001363890
Location:5UTRS;EXON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001594523 CLINVAR
dbSNP (RS) rs279558 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene JAGN1 CLINVAR
OMIM 616012 CLINVAR