RGD:156369911 Rat Genome Database

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Variant: RGD:156369911 -  Homo sapiens

RGD ID: 156369911
ClinVar ID: CV2174359
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: ARIH1  
Reference Nucleotide: TTTTTTCTC
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 15 72,875,530 - 72,875,539
GRCh38 15 72,583,189 - 72,583,198
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005744.5:c.1590-17_1590-9del
NC_000015.10:g.72583191_72583199del
NC_000015.9:g.72875529_72875537del
NC_000015.9:g.72875532_72875540del
 03/08/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003049619 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARIH1 CLINVAR
OMIM 605624 CLINVAR