RGD:156161629 Rat Genome Database

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Variant: RGD:156161629 -  Homo sapiens

RGD ID: 156161629
ClinVar ID: CV2033898
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 6,693,501
GRCh38 19 6,693,490
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.3155-3C>A
LRG_27:g.32162C>A
NG_009557.1:g.32162C>A
NC_000019.10:g.6693490G>T
More... 		06/13/2022 intron variant uncertain significance none provided

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

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


Additional Information

Database Acc Id Source(s)
ClinVar RCV002741566 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR