rs551161869 Rat Genome Database

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Variant: rs551161869 -  Homo sapiens

RGD ID: 126923914
RS ID: rs551161869
ClinVar ID: CV1041744
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 96,940,990
GRCh38 2 96,275,252
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.6267+5G>A
NG_016973.1:g.35308G>A
NC_000002.12:g.96275252C>T
NC_000002.11:g.96940990C>T
 07/26/2022 intron variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SNRNP200
Accession:NM_014014
Location:INTRON

.
PMID:9536098   PMID:17576681   PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV001366402 CLINVAR
dbSNP (RS) rs551161869 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR