RGD:156216938 Rat Genome Database

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Variant: RGD:156216938 -  Homo sapiens

RGD ID: 156216938
ClinVar ID: CV2084511
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 96,949,466
GRCh38 2 96,283,728
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.4585-15C>A
NG_016973.1:g.26832C>A
NC_000002.12:g.96283728G>T
NC_000002.11:g.96949466G>T
 11/24/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SNRNP200
Accession:NM_014014
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002853057 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR