rs3745368 Rat Genome Database

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Variant: rs3745368 -  Homo sapiens

RGD ID: 8558328
RS ID: rs3745368
ClinVar ID: CV19923
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RETN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 7,735,297
GRCh38 19 7,670,411
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001385727.1:c.*62G>A
NC_000019.9:g.7735297G>A
NM_001385726.1:c.*62G>A
NG_023447.1:g.6326G>A
More... 		04/27/2007 3 prime utr variant risk factor
Disease Annotations     Click to see Annotation Detail View

GWAS Catalog Data
GWAS Catalog Study Disease Trait Study Size Risk Allele Risk Allele Frequency P Value P Value MLOG SNP Passing QC Reported Odds Ratio or Beta-coefficient Ontology Accession PubMed
GCST90161609 Resistin levels 2,935 Qatari ancestry individuals A 0.0262351 4E-13 12.397940008672037 NR [10004359] 0.618764 resistin measurement (EFO:0004819)
 PMID:36168886

Variant Details
Variant Transcripts
Gene Symbol:RETN
Accession:NM_001193374
Location:3UTRS;EXON

Gene Symbol:RETN
Accession:NM_001385726
Location:3UTRS;EXON

Gene Symbol:RETN
Accession:NM_001385727
Location:3UTRS;EXON

Gene Symbol:RETN
Accession:NM_020415
Location:3UTRS;EXON

Gene Symbol:RETN
Accession:NM_001385725
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:11558907   PMID:12629116  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000005160 CLINVAR
  RCV000005161 CLINVAR
dbSNP (RS) rs3745368 CLINVAR
GWAS Catalog GCST90161609 GWAS Catalog
MedGen C3837967 CLINVAR
NCBI Gene RETN CLINVAR
OMIM 605565 CLINVAR
OMIM Allele 605565.0001 CLINVAR