rs11569511 Rat Genome Database

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Variant: rs11569511 -  Homo sapiens

RGD ID: 150469110
RS ID: rs11569511
ClinVar ID: CV1219019
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 6,690,571
GRCh38 19 6,690,560
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009557.1:g.35092G>A
NM_000064.4:c.3489+69G>A
LRG_27:g.35092G>A
NC_000019.10:g.6690560C>T
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 RCV001614771 CLINVAR
dbSNP (RS) rs11569511 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR