RGD:156014399 Rat Genome Database

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Variant: RGD:156014399 -  Homo sapiens

RGD ID: 156014399
ClinVar ID: CV2123125
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARIH1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 72,864,525
GRCh38 15 72,572,184
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005744.5:c.1215+19G>A
NC_000015.10:g.72572184G>A
NC_000015.9:g.72864525G>A
 11/14/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ARIH1
Accession:NM_005744
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002975822 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARIH1 CLINVAR
OMIM 605624 CLINVAR