rs1552223

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0228 (6661/29118,TOPMED)
G==0215 (1075/5008,1000G)
G==0413 (1590/3854,ALSPAC)
G==0395 (1464/3708,TWINSUK)
chr19:41020047 (GRCh38.p7) (19q13.2)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 19NC_000019.10:g.41020047G>A
GRCh37.p13 chr 19NC_000019.9:g.41525952G>A
CYP2B6 RefSeqGeneNG_007929.1:g.33749G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.017A=0.983
1000GenomesAmericanSub694G=0.190A=0.810
1000GenomesEast AsianSub1008G=0.326A=0.674
1000GenomesEuropeSub1006G=0.386A=0.614
1000GenomesGlobalStudy-wide5008G=0.215A=0.785
1000GenomesSouth AsianSub978G=0.210A=0.790
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.413A=0.587
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.228A=0.771
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.395A=0.605
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res
24885815Genetic variation in the CYP2B6 gene is related to circulating 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) concentrations: an observational population-based study.Penell JEnviron Health

P-Value

SNP ID p-value Traits Study
rs15522230.000313alcohol dependence21314694

eQTL of rs1552223 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs1552223 in Fetal Brain

Probe ID Position Gene beta p-value
cg27089200chr19:41531976-0.04649309660593945.5396e-10

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.