rs769440522 Rat Genome Database

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Variant: rs769440522 -  Homo sapiens

RGD ID: 126747352
RS ID: rs769440522
ClinVar ID: CV1013608
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COMP  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 18,893,774
GRCh38 19 18,782,964
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.2228-3C>T
NG_007070.1:g.13341C>T
NC_000019.10:g.18782964G>A
NC_000019.9:g.18893774G>A
02/29/2020 intron variant uncertain significance none provided

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

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001315336 CLINVAR
dbSNP (RS) rs769440522 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COMP CLINVAR
OMIM 600310 CLINVAR