rs11752804

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0068 (2052/29964,GnomAD)
A=0056 (1643/29118,TOPMED)
A=0043 (215/5008,1000G)
A=0112 (432/3854,ALSPAC)
A=0102 (379/3708,TWINSUK)
chr6:85318963 (GRCh38.p7) (6q14.3)
AD
GWASdb2
1   publication(s)
See rs on genome
2 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.85318963G>A
GRCh37.p13 chr 6NC_000006.11:g.86028681G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.988A=0.012
1000GenomesAmericanSub694G=0.970A=0.030
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=0.891A=0.109
1000GenomesGlobalStudy-wide5008G=0.957A=0.043
1000GenomesSouth AsianSub978G=0.930A=0.070
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.888A=0.112
The Genome Aggregation DatabaseAfricanSub8726G=0.979A=0.021
The Genome Aggregation DatabaseAmericanSub838G=0.950A=0.050
The Genome Aggregation DatabaseEast AsianSub1622G=1.000A=0.000
The Genome Aggregation DatabaseEuropeSub18476G=0.902A=0.097
The Genome Aggregation DatabaseGlobalStudy-wide29964G=0.931A=0.068
The Genome Aggregation DatabaseOtherSub302G=0.890A=0.110
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.943A=0.056
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.898A=0.102
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs117528040.000013alcoholismpha002892
rs117528040.000013alcohol dependence20201924
rs117528040.00031alcohol dependence(Early Onset)20201924

eQTL of rs11752804 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 rs11752804 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 )
chr68599293885993521E081-35160
chr68599375885993812E081-34869