RGD:21066615 Rat Genome Database

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Variant: RGD:21066615 -  Homo sapiens

RGD ID: 21066615
RS ID: rs1601059553
ClinVar ID: CV797778
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COMP  LOC127890904  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 18,900,745
GRCh38 19 18,789,936
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000095.3:c.390+6C>T
NG_007070.1:g.6370C>T
NC_000019.10:g.18789936G>A
NC_000019.9:g.18900745G>A
 10/01/2018 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:COMP
Accession:NM_000095
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000996826 CLINVAR
dbSNP (RS) rs1601059553 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COMP CLINVAR
OMIM 600310 CLINVAR