RGD:405107686 Rat Genome Database

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Variant: RGD:405107686 -  Homo sapiens

RGD ID: 405107686
ClinVar ID: CV3136281
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARIH1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 72,847,720
GRCh38 15 72,555,379
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005744.5:c.681+16T>C
NC_000015.10:g.72555379T>C
NC_000015.9:g.72847720T>C
 07/20/2023 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 RCV003835627 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARIH1 CLINVAR
OMIM 605624 CLINVAR