rs11157218

Homo sapiens
A>G / A>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0265 (7917/29792,GnomAD)
T=0330 (1653/5008,1000G)
chr14:41304577 (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.41304577A>G
GRCh38.p7 chr 14NC_000014.9:g.41304577A>T
GRCh37.p13 chr 14NC_000014.8:g.41773780A>G
GRCh37.p13 chr 14NC_000014.8:g.41773780A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.831T=0.169
1000GenomesAmericanSub694A=0.710T=0.290
1000GenomesEast AsianSub1008A=0.468T=0.532
1000GenomesEuropeSub1006A=0.732T=0.268
1000GenomesGlobalStudy-wide5008A=0.670T=0.330
1000GenomesSouth AsianSub978A=0.570T=0.430
The Genome Aggregation DatabaseAfricanSub8700A=0.786T=0.213
The Genome Aggregation DatabaseAmericanSub834A=0.730T=0.27,
The Genome Aggregation DatabaseEast AsianSub1580A=0.498T=0.502
The Genome Aggregation DatabaseEuropeSub18376A=0.726T=0.270
The Genome Aggregation DatabaseGlobalStudy-wide29792A=0.732T=0.265
The Genome Aggregation DatabaseOtherSub302A=0.740T=0.25,
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
rs111572180.000427nicotine dependence17158188

eQTL of rs11157218 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 rs11157218 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.