rs1782167

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0203 (5931/29118,TOPMED)
G==0206 (1033/5008,1000G)
G==0284 (1096/3854,ALSPAC)
G==0279 (1033/3708,TWINSUK)
chr14:41204511 (GRCh38.p7) (14q21.1)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 14NC_000014.9:g.41204511G>A
GRCh37.p13 chr 14NC_000014.8:g.41673714G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.088A=0.912
1000GenomesAmericanSub694G=0.210A=0.790
1000GenomesEast AsianSub1008G=0.189A=0.811
1000GenomesEuropeSub1006G=0.261A=0.739
1000GenomesGlobalStudy-wide5008G=0.206A=0.794
1000GenomesSouth AsianSub978G=0.320A=0.680
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.284A=0.716
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.203A=0.796
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.279A=0.721
PMID Title Author Journal
17158188Novel genes identified in a high-density genome wide association study for nicotine dependence.Bierut LJHum Mol Genet

P-Value

SNP ID p-value Traits Study
rs17821670.00033nicotine dependence17158188

eQTL of rs1782167 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 rs1782167 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.