rs11569513 Rat Genome Database

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Variant: rs11569513 -  Homo sapiens

RGD ID: 150511435
RS ID: rs11569513
ClinVar ID: CV1229462
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 6,690,460
GRCh38 19 6,690,449
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.6690449C>G
NC_000019.9:g.6690460C>G
NM_000064.4:c.3489+180G>C
LRG_27:g.35203G>C
More... 		06/18/2021 intron variant benign none provided

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

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001637391 CLINVAR
dbSNP (RS) rs11569513 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR