rs11076221

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
A==0085 (2552/29970,GnomAD)
A==0094 (2747/29118,TOPMED)
A==0096 (481/5008,1000G)
A==0074 (287/3854,ALSPAC)
A==0077 (285/3708,TWINSUK)
chr16:51927631 (GRCh38.p7) (16q12.1)
AD
GWASCatalog
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 16NC_000016.10:g.51927631A>G
GRCh37.p13 chr 16NC_000016.9:g.51961543A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.156G=0.844
1000GenomesAmericanSub694A=0.030G=0.970
1000GenomesEast AsianSub1008A=0.092G=0.908
1000GenomesEuropeSub1006A=0.066G=0.934
1000GenomesGlobalStudy-wide5008A=0.096G=0.904
1000GenomesSouth AsianSub978A=0.100G=0.900
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.074G=0.926
The Genome Aggregation DatabaseAfricanSub8714A=0.148G=0.852
The Genome Aggregation DatabaseAmericanSub838A=0.040G=0.960
The Genome Aggregation DatabaseEast AsianSub1620A=0.111G=0.889
The Genome Aggregation DatabaseEuropeSub18496A=0.055G=0.944
The Genome Aggregation DatabaseGlobalStudy-wide29970A=0.085G=0.914
The Genome Aggregation DatabaseOtherSub302A=0.060G=0.940
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.094G=0.905
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.077G=0.923
PMID Title Author Journal
26365420The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.Mbarek HAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs110762219E-06alcohol dependence26365420

eQTL of rs11076221 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 rs11076221 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 )
chr165197287751973815E07011334
chr165197403951974079E07012496
chr165197416751974533E07012624
chr165200127952001349E07039736
chr165200143952001511E07039896
chr165200157952001923E07040036
chr165200223252002292E07040689
chr165200238352002464E07040840
chr165200278652002894E07041243
chr165197287751973815E08111334
chr165197403951974079E08112496
chr165197416751974533E08112624
chr165200143952001511E08139896
chr165200157952001923E08140036
chr165197287751973815E08211334
chr165197403951974079E08212496
chr165198739351987530E08225850
chr165200157952001923E08240036
chr165200575052006185E08244207