rs11157219

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0227 (6789/29914,GnomAD)
G=0214 (6240/29118,TOPMED)
G=0208 (1042/5008,1000G)
G=0282 (1087/3854,ALSPAC)
G=0282 (1047/3708,TWINSUK)
chr14:41313498 (GRCh38.p7) (14q21.1)
ND
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 14NC_000014.9:g.41313498A>G
GRCh37.p13 chr 14NC_000014.8:g.41782701A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.887G=0.113
1000GenomesAmericanSub694A=0.790G=0.210
1000GenomesEast AsianSub1008A=0.834G=0.166
1000GenomesEuropeSub1006A=0.743G=0.257
1000GenomesGlobalStudy-wide5008A=0.792G=0.208
1000GenomesSouth AsianSub978A=0.670G=0.330
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.718G=0.282
The Genome Aggregation DatabaseAfricanSub8714A=0.831G=0.169
The Genome Aggregation DatabaseAmericanSub836A=0.830G=0.170
The Genome Aggregation DatabaseEast AsianSub1610A=0.807G=0.193
The Genome Aggregation DatabaseEuropeSub18452A=0.740G=0.259
The Genome Aggregation DatabaseGlobalStudy-wide29914A=0.773G=0.227
The Genome Aggregation DatabaseOtherSub302A=0.750G=0.250
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.785G=0.214
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.718G=0.282
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
rs111572198.78E-05nicotine dependence17158188

eQTL of rs11157219 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 rs11157219 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 )
chr144175450541754720E070-27981
chr144174720041747372E081-35329
chr144174720041747372E082-35329