rs77544380 Rat Genome Database

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Variant: rs77544380 -  Homo sapiens

RGD ID: 150447057
RS ID: rs77544380
ClinVar ID: CV1250764
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLCO2A1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 133,692,193
GRCh38 3 133,973,349
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_841t1:c.397+314A>C
NM_005630.3:c.397+314A>C
LRG_841:g.83836A>C
NG_031964.3:g.83836A>C
More... 		11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLCO2A1
Accession:NM_005630
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001667269 CLINVAR
dbSNP (RS) rs77544380 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLCO2A1 CLINVAR
OMIM 601460 CLINVAR