rs1785039

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0225 (6744/29950,GnomAD)
G=0229 (6672/29118,TOPMED)
G=0249 (1249/5008,1000G)
G=0189 (730/3854,ALSPAC)
G=0193 (717/3708,TWINSUK)
chr11:128030684 (GRCh38.p7) (11q24.3)
AD
GWASdb2
1   publication(s)
See rs on genome
2 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 11NC_000011.10:g.128030684A>G
GRCh37.p13 chr 11NC_000011.9:g.127900579A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.720G=0.280
1000GenomesAmericanSub694A=0.810G=0.190
1000GenomesEast AsianSub1008A=0.694G=0.306
1000GenomesEuropeSub1006A=0.798G=0.202
1000GenomesGlobalStudy-wide5008A=0.751G=0.249
1000GenomesSouth AsianSub978A=0.760G=0.240
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.811G=0.189
The Genome Aggregation DatabaseAfricanSub8706A=0.701G=0.299
The Genome Aggregation DatabaseAmericanSub838A=0.820G=0.180
The Genome Aggregation DatabaseEast AsianSub1614A=0.721G=0.279
The Genome Aggregation DatabaseEuropeSub18490A=0.813G=0.186
The Genome Aggregation DatabaseGlobalStudy-wide29950A=0.774G=0.225
The Genome Aggregation DatabaseOtherSub302A=0.710G=0.290
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.770G=0.229
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.807G=0.193
PMID Title Author Journal
21529783A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.Heath ACBiol Psychiatry

P-Value

SNP ID p-value Traits Study
rs17850396.1E-05alcoholism (heaviness of drinking)21529783

eQTL of rs1785039 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 rs1785039 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.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr11127940765127940822E07040186
chr11127941221127941271E07040642