rs12148800 Rat Genome Database

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Variant: rs12148800 -  Homo sapiens

RGD ID: 155882381
RS ID: rs12148800
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: UNC13C  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh38 15 54,028,572
JBrowse: View Region in Genome Browser (JBrowse)
Model



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs12148800Humaneducational attainment  IAGP 405850206 GWAS_CATALOGPMID:35361970
Data has come from the GWAS Catalog   
QTL
GWAS Catalog Study
Disease Trait
Study Size
Risk Allele
Risk Allele Frequency
P Value
P Value MLOG
Peak Marker
Reported Odds Ratio or Beta-coefficient
Ontology Accession
PubMed
GWAS1434385_H GCST90105038 Educational attainment 3,037,499 European ancestry individuals T 0.5174 2E-7 6.699 rs12148800 0.00546502 educational attainment (EFO:0011015)
 PMID:35361970

Gene Symbol:UNC13C
Accession:XM_017022225
Location:5UTRS;INTRON

Gene Symbol:UNC13C
Accession:NM_001080534
Location:INTRON

Gene Symbol:UNC13C
Accession:XM_017022220
Location:INTRON

Gene Symbol:UNC13C
Accession:XM_017022221
Location:INTRON

Gene Symbol:UNC13C
Accession:XM_017022222
Location:INTRON

Gene Symbol:UNC13C
Accession:NM_001329919
Location:INTRON

Gene Symbol:UNC13C
Accession:XM_047432538
Location:INTRON

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Database
Acc Id
Source(s)
GWAS Catalog GCST90105038 GWAS Catalog