rs7113885

Homo sapiens
A>C / A>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0175 (5242/29918,GnomAD)
T=0189 (946/5008,1000G)
chr11:95562213 (GRCh38.p7) (11q21)
ND
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 11NC_000011.10:g.95562213A>C
GRCh38.p7 chr 11NC_000011.10:g.95562213A>T
GRCh37.p13 chr 11NC_000011.9:g.95295377A>C
GRCh37.p13 chr 11NC_000011.9:g.95295377A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.661C=0.154
1000GenomesAmericanSub694A=0.550C=0.07,
1000GenomesEast AsianSub1008A=0.705C=0.133
1000GenomesEuropeSub1006A=0.793C=0.049
1000GenomesGlobalStudy-wide5008A=0.703C=0.108
1000GenomesSouth AsianSub978A=0.770C=0.11,
The Genome Aggregation DatabaseAfricanSub8706A=0.695C=0.145
The Genome Aggregation DatabaseAmericanSub830A=0.540C=0.07,
The Genome Aggregation DatabaseEast AsianSub1598A=0.676C=0.113
The Genome Aggregation DatabaseEuropeSub18482A=0.775C=0.053
The Genome Aggregation DatabaseGlobalStudy-wide29918A=0.741C=0.083
The Genome Aggregation DatabaseOtherSub302A=0.850C=0.02,
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
rs71138850.000137nicotine dependence17158188

eQTL of rs7113885 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 rs7113885 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 )
chr114168735441687416E070-11988
chr114168745941687503E070-11901
chr114168865341688717E070-10687