rs2866619

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0112 (3350/29906,GnomAD)
A=0124 (3627/29118,TOPMED)
A=0199 (998/5008,1000G)
A=0031 (118/3854,ALSPAC)
A=0031 (115/3708,TWINSUK)
chr16:76218244 (GRCh38.p7) (16q23.1)
ND
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 16NC_000016.10:g.76218244G>A
GRCh37.p13 chr 16NC_000016.9:g.76252142G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.750A=0.250
1000GenomesAmericanSub694G=0.900A=0.100
1000GenomesEast AsianSub1008G=0.605A=0.395
1000GenomesEuropeSub1006G=0.965A=0.035
1000GenomesGlobalStudy-wide5008G=0.801A=0.199
1000GenomesSouth AsianSub978G=0.830A=0.170
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.969A=0.031
The Genome Aggregation DatabaseAfricanSub8708G=0.784A=0.216
The Genome Aggregation DatabaseAmericanSub834G=0.900A=0.100
The Genome Aggregation DatabaseEast AsianSub1584G=0.586A=0.414
The Genome Aggregation DatabaseEuropeSub18478G=0.960A=0.039
The Genome Aggregation DatabaseGlobalStudy-wide29906G=0.888A=0.112
The Genome Aggregation DatabaseOtherSub302G=0.980A=0.020
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.875A=0.124
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.969A=0.031
PMID Title Author Journal
20158304A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.Lind PATwin Res Hum Genet

P-Value

SNP ID p-value Traits Study
rs28666192.38E-05alcohol and nictotine co-dependence20158304

eQTL of rs2866619 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 rs2866619 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 )
chr167622771276229397E068-22745
chr167622771276229397E071-22745
chr167623330876234058E074-18084