RGD:28869510 Rat Genome Database

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Variant: RGD:28869510 -  Homo sapiens

RGD ID: 28869510
RS ID: rs886634767
ClinVar ID: CV882095
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127891602  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 42,364,310
GRCh38 19 41,860,240
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_007080.3:g.5323G>A
NC_000019.9:g.42364310G>A
NG_141460.1:g.383G>A
NC_000019.10:g.41860240G>A
More... 		01/13/2018 uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001130691 CLINVAR
dbSNP (RS) rs886634767 CLINVAR
MedGen C2676137 CLINVAR
NCBI Gene RPS19 CLINVAR
OMIM 105650 CLINVAR
  603474 CLINVAR