rs12232841

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0463 (13880/29946,GnomAD)
G=0425 (12384/29118,TOPMED)
G=0458 (2292/5008,1000G)
T==0419 (1615/3854,ALSPAC)
T==0410 (1520/3708,TWINSUK)
chr19:21674425 (GRCh38.p7) (19p12)
AD
GWASdb2
1   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.21674425T>G
GRCh37.p13 chr 19NC_000019.9:g.21857227T>G
GRCh38.p7 chr 19 alt locus HSCHR19_2_CTG2NW_003315964.2:g.35622T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.893G=0.107
1000GenomesAmericanSub694T=0.370G=0.630
1000GenomesEast AsianSub1008T=0.438G=0.562
1000GenomesEuropeSub1006T=0.425G=0.575
1000GenomesGlobalStudy-wide5008T=0.542G=0.458
1000GenomesSouth AsianSub978T=0.420G=0.580
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.419G=0.581
The Genome Aggregation DatabaseAfricanSub8716T=0.834G=0.166
The Genome Aggregation DatabaseAmericanSub834T=0.380G=0.620
The Genome Aggregation DatabaseEast AsianSub1616T=0.389G=0.611
The Genome Aggregation DatabaseEuropeSub18478T=0.419G=0.581
The Genome Aggregation DatabaseGlobalStudy-wide29946T=0.536G=0.463
The Genome Aggregation DatabaseOtherSub302T=0.350G=0.650
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.574G=0.425
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.410G=0.590
PMID Title Author Journal
21703634A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.Wang KSJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs122328415.93E-05alcohol dependence21703634

eQTL of rs12232841 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G1.4096e-14-35097Cerebellum
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G2.0232e-15-35097Frontal_Cortex_BA9
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G8.0717e-13-35097Hypothalamus
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G1.0023e-12-35097Cerebellar_Hemisphere
Chr19:21857227VN1R84PENSG00000268117.1T>G1.0266e-19-45610Cerebellar_Hemisphere
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G1.9463e-8-35097Brain_Spinal_cord_cervical
Chr19:21857227RP11-420K14.3ENSG00000268535.1T>G3.6263e-9-35097Substantia_nigra

meQTL of rs12232841 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

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