rs777114537 Rat Genome Database

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Variant: rs777114537 -  Homo sapiens

RGD ID: 151852711
RS ID: rs777114537
ClinVar ID: CV1501959
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127398749  SLCO2A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 133,661,443
GRCh38 3 133,942,599
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_841t1:c.1625+6T>C
NM_005630.3:c.1625+6T>C
LRG_841:g.114586T>C
NG_031964.3:g.114586T>C
More... 		11/16/2022 intron variant likely pathogenic|uncertain significance none provided

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

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


Additional Information

Database Acc Id Source(s)
ClinVar RCV001937572 CLINVAR
dbSNP (RS) rs777114537 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLCO2A1 CLINVAR
OMIM 601460 CLINVAR