rs768889200 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: rs768889200 -  Homo sapiens

RGD ID: 127318748
RS ID: rs768889200
ClinVar ID: CV1134211
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 96,950,911
GRCh38 2 96,285,173
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.4164+7C>T
NG_016973.1:g.25387C>T
NC_000002.12:g.96285173G>A
NC_000002.11:g.96950911G>A
11/01/2022 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 RCV001483612 CLINVAR
dbSNP (RS) rs768889200 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR