RGD:11658733 Rat Genome Database

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Variant: RGD:11658733 -  Homo sapiens

RGD ID: 11658733
RS ID: rs886054468
ClinVar ID: CV349028
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127891602  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 42,364,286
GRCh38 19 41,860,216
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
NC_000019.10:g.41860216C>T
NC_000019.9:g.42364286C>T
NG_007080.3:g.5299C>T
LRG_1144:g.5299C>T
More... 		06/14/2016 2kb upstream variant uncertain significance neonatal/infancy
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000351569 CLINVAR
dbSNP (RS) rs886054468 CLINVAR
MedGen C2676137 CLINVAR
NCBI Gene RPS19 CLINVAR
OMIM 105650 CLINVAR
  603474 CLINVAR