rs3787050 Rat Genome Database

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Variant: rs3787050 -  Homo sapiens

RGD ID: 150504373
RS ID: rs3787050
ClinVar ID: CV1212670
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COMP  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 18,900,360
GRCh38 19 18,789,551
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.391-254C>T
NG_007070.1:g.6755C>T
NC_000019.10:g.18789551G>A
NC_000019.9:g.18900360G>A
 08/09/2018 intron variant benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001595545 CLINVAR
dbSNP (RS) rs3787050 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COMP CLINVAR
OMIM 600310 CLINVAR