rs774669313 Rat Genome Database

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Variant: rs774669313 -  Homo sapiens

RGD ID: 152059101
RS ID: rs774669313
ClinVar ID: CV1595862
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 96,947,676
GRCh38 2 96,281,938
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.4916-16C>T
NG_016973.1:g.28622C>T
NC_000002.12:g.96281938G>A
NC_000002.11:g.96947676G>A
 08/17/2023 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 RCV002090042 CLINVAR
dbSNP (RS) rs774669313 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR