rs199993487 Rat Genome Database

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Variant: rs199993487 -  Homo sapiens

RGD ID: 127316169
RS ID: rs199993487
ClinVar ID: CV1154236
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126806272  SNRNP200  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 96,945,316
GRCh38 2 96,279,578
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.5025-19T>C
NG_016973.1:g.30982T>C
NC_000002.12:g.96279578A>G
NC_000002.11:g.96945316A>G
 01/11/2024 intron variant 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 RCV001520349 CLINVAR
dbSNP (RS) rs199993487 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126806272 CLINVAR
  SNRNP200 CLINVAR
OMIM 601664 CLINVAR