rs2829746

Homo sapiens
G>A
LINC00158 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0105 (3143/29940,GnomAD)
G==0089 (2596/29118,TOPMED)
G==0173 (868/5008,1000G)
G==0080 (307/3854,ALSPAC)
G==0078 (290/3708,TWINSUK)
chr21:25425777 (GRCh38.p7) (21q21.2)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 21NC_000021.9:g.25425777G>A
GRCh37.p13 chr 21NC_000021.8:g.26798089G>A

Gene: LINC00158, long intergenic non-protein coding RNA 158(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LINC00158 transcriptNR_024027.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.136A=0.864
1000GenomesAmericanSub694G=0.030A=0.970
1000GenomesEast AsianSub1008G=0.411A=0.589
1000GenomesEuropeSub1006G=0.083A=0.917
1000GenomesGlobalStudy-wide5008G=0.173A=0.827
1000GenomesSouth AsianSub978G=0.170A=0.830
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.080A=0.920
The Genome Aggregation DatabaseAfricanSub8726G=0.120A=0.880
The Genome Aggregation DatabaseAmericanSub836G=0.050A=0.950
The Genome Aggregation DatabaseEast AsianSub1610G=0.427A=0.573
The Genome Aggregation DatabaseEuropeSub18466G=0.074A=0.926
The Genome Aggregation DatabaseGlobalStudy-wide29940G=0.105A=0.895
The Genome Aggregation DatabaseOtherSub302G=0.010A=0.990
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.089A=0.910
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.078A=0.922
PMID Title Author Journal
22377092ANAPC1 and SLCO3A1 are associated with nicotine dependence: meta-analysis of genome-wide association studies.Wang KSDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs28297463.93E-05nicotine dependence (smoking)22377092

eQTL of rs2829746 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 rs2829746 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.