rs1389625 Rat Genome Database

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Variant: rs1389625 -  Homo sapiens

RGD ID: 150499953
RS ID: rs1389625
ClinVar ID: CV1224691
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 6,684,142
GRCh38 19 6,684,131
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.4172+257T>C
LRG_27:g.41521T>C
NG_009557.1:g.41521T>C
NC_000019.10:g.6684131A>G
More... 		06/18/2021 intron variant benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001620523 CLINVAR
dbSNP (RS) rs1389625 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR