rs4859365

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0457 (13649/29818,GnomAD)
G==0460 (13409/29118,TOPMED)
G==0450 (2252/5008,1000G)
G==0491 (1893/3854,ALSPAC)
A=0498 (1845/3708,TWINSUK)
chr4:35520910 (GRCh38.p7) (4p15.1)
ND
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.35520910G>A
GRCh37.p13 chr 4NC_000004.11:g.35522532G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.401A=0.599
1000GenomesAmericanSub694G=0.530A=0.470
1000GenomesEast AsianSub1008G=0.300A=0.700
1000GenomesEuropeSub1006G=0.465A=0.535
1000GenomesGlobalStudy-wide5008G=0.450A=0.550
1000GenomesSouth AsianSub978G=0.600A=0.400
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.491A=0.509
The Genome Aggregation DatabaseAfricanSub8678G=0.412A=0.588
The Genome Aggregation DatabaseAmericanSub828G=0.570A=0.430
The Genome Aggregation DatabaseEast AsianSub1612G=0.261A=0.739
The Genome Aggregation DatabaseEuropeSub18400G=0.492A=0.507
The Genome Aggregation DatabaseGlobalStudy-wide29818G=0.457A=0.542
The Genome Aggregation DatabaseOtherSub300G=0.420A=0.580
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.460A=0.539
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.502A=0.498
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
rs48593657.72E-05nicotine dependence17158188

eQTL of rs4859365 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 rs4859365 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 )
chr43552673735526787E0744205
chr43553670135536912E08214169
chr43553699835537160E08214466


Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr43552687235526986E0684340
chr43552703435527236E0684502
chr43552753335527608E0685001
chr43552687235526986E0694340
chr43552703435527236E0694502
chr43552687235526986E0714340
chr43552703435527236E0714502
chr43552753335527608E0715001
chr43552687235526986E0724340
chr43552703435527236E0724502
chr43552687235526986E0734340
chr43552703435527236E0734502
chr43552687235526986E0744340
chr43552703435527236E0744502