rs369773058 Rat Genome Database

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Variant: rs369773058 -  Homo sapiens

RGD ID: 152090686
RS ID: rs369773058
ClinVar ID: CV1525613
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 6,680,150
GRCh38 19 6,680,139
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000064.4:c.4456+19G>A
LRG_27:g.45513G>A
NG_009557.1:g.45513G>A
NC_000019.10:g.6680139C>T
More... 		01/08/2024 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:C3
Accession:NM_000064
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002150550 CLINVAR
dbSNP (RS) rs369773058 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR