rs6766181

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0438 (13112/29920,GnomAD)
T=0430 (12526/29118,TOPMED)
T=0398 (1991/5008,1000G)
C==0490 (1889/3854,ALSPAC)
T=0494 (1833/3708,TWINSUK)
chr3:27058799 (GRCh38.p7) (3p24.1)
AD
GWASdb2
1   publication(s)
See rs on genome
10 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.27058799C>T
GRCh37.p13 chr 3NC_000003.11:g.27100290C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.645T=0.355
1000GenomesAmericanSub694C=0.510T=0.490
1000GenomesEast AsianSub1008C=0.794T=0.206
1000GenomesEuropeSub1006C=0.491T=0.509
1000GenomesGlobalStudy-wide5008C=0.602T=0.398
1000GenomesSouth AsianSub978C=0.530T=0.470
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.490T=0.510
The Genome Aggregation DatabaseAfricanSub8714C=0.634T=0.366
The Genome Aggregation DatabaseAmericanSub834C=0.570T=0.430
The Genome Aggregation DatabaseEast AsianSub1596C=0.807T=0.193
The Genome Aggregation DatabaseEuropeSub18474C=0.507T=0.492
The Genome Aggregation DatabaseGlobalStudy-wide29920C=0.561T=0.438
The Genome Aggregation DatabaseOtherSub302C=0.450T=0.550
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.569T=0.430
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.506T=0.494
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
rs67661812.4E-05alcoholism (heaviness of drinking)21529783

eQTL of rs6766181 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 rs6766181 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 )
chr32707568827076352E067-23938
chr32707656227076618E067-23672
chr32707568827076352E068-23938
chr32707568827076352E069-23938
chr32707656227076618E069-23672
chr32707568827076352E071-23938
chr32712328327123473E07222993
chr32712328327123473E07422993
chr32712353727123778E07423247
chr32712380427123983E08223514