rs3092155

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0217 (6517/29958,GnomAD)
G=0140 (701/5008,1000G)
G=0264 (1018/3854,ALSPAC)
G=0257 (954/3708,TWINSUK)
chr20:40413231 (GRCh38.p7) (20q12)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 20NC_000020.11:g.40413231A>G
GRCh37.p13 chr 20NC_000020.10:g.39041871A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.947G=0.053
1000GenomesAmericanSub694A=0.810G=0.190
1000GenomesEast AsianSub1008A=0.891G=0.109
1000GenomesEuropeSub1006A=0.718G=0.282
1000GenomesGlobalStudy-wide5008A=0.860G=0.140
1000GenomesSouth AsianSub978A=0.890G=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.736G=0.264
The Genome Aggregation DatabaseAfricanSub8722A=0.921G=0.079
The Genome Aggregation DatabaseAmericanSub838A=0.790G=0.210
The Genome Aggregation DatabaseEast AsianSub1622A=0.883G=0.117
The Genome Aggregation DatabaseEuropeSub18474A=0.706G=0.293
The Genome Aggregation DatabaseGlobalStudy-wide29958A=0.782G=0.217
The Genome Aggregation DatabaseOtherSub302A=0.850G=0.150
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.743G=0.257
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
rs30921554.37E-06alcohol and nictotine co-dependence20158304

eQTL of rs3092155 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 rs3092155 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.