rs2798983

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
C=0238 (7125/29842,GnomAD)
C=0220 (6422/29118,TOPMED)
C=0231 (1158/5008,1000G)
C=0283 (1090/3854,ALSPAC)
C=0283 (1048/3708,TWINSUK)
chr14:41303030 (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.41303030C>T
GRCh37.p13 chr 14NC_000014.8:g.41772233T>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.874C==0.126
1000GenomesAmericanSub694T=0.790C==0.210
1000GenomesEast AsianSub1008T=0.750C==0.250
1000GenomesEuropeSub1006T=0.736C==0.264
1000GenomesGlobalStudy-wide5008T=0.769C==0.231
1000GenomesSouth AsianSub978T=0.670C==0.330
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.717C==0.283
The Genome Aggregation DatabaseAfricanSub8720T=0.817C==0.183
The Genome Aggregation DatabaseAmericanSub832T=0.830C==0.170
The Genome Aggregation DatabaseEast AsianSub1586T=0.740C==0.260
The Genome Aggregation DatabaseEuropeSub18402T=0.733C==0.266
The Genome Aggregation DatabaseGlobalStudy-wide29842T=0.761C==0.238
The Genome Aggregation DatabaseOtherSub302T=0.750C==0.250
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.779C==0.220
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.717C==0.283
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
rs27989834.77E-05nicotine dependence17158188

eQTL of rs2798983 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 rs2798983 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 )
chr144175450541754720E070-17513
chr144174720041747372E081-24861
chr144174720041747372E082-24861