rs10106898 Rat Genome Database

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Variant: rs10106898 -  Homo sapiens

RGD ID: 406204550
RS ID: rs10106898
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 8 96,095,722
JBrowse: View Region in Genome Browser (JBrowse)
Model



Disease Annotations     Click to see Annotation Detail View
cleft lip  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Cleft lip  (IAGP)
GWAS QTLs Related by Peak Marker
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
GWAS1173954_H GCST005654 Cleft lip with or without cleft palate (maternal periconceptional cigarette smoking interaction) up to 825 European ancestry case-parent trios, up to 1,024 Asian ancestry case-parent trios, up to 59 case-parent trios ? NR 0.000004 5.398 rs10106898 3.448276 tobacco smoke exposure measurement (EFO:0009115)
cleft lip (EFO:0003959)
 PMID:29535761

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST005654 GWAS Catalog