rs1760803

Homo sapiens
A>T
None
Check p-value
SNV (Single Nucleotide Variation)
A==0417 (12141/29118,TOPMED)
T=0488 (2442/5008,1000G)
A==0469 (1806/3854,ALSPAC)
A==0458 (1699/3708,TWINSUK)
chr1:154285418 (GRCh38.p7) (1q21.3)
ND
GWASCatalog
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.154285418A>T
GRCh37.p13 chr 1NC_000001.10:g.154257894A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.343T=0.657
1000GenomesAmericanSub694A=0.650T=0.350
1000GenomesEast AsianSub1008A=0.525T=0.475
1000GenomesEuropeSub1006A=0.449T=0.551
1000GenomesGlobalStudy-wide5008A=0.512T=0.488
1000GenomesSouth AsianSub978A=0.700T=0.300
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.469T=0.531
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.417T=0.583
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.458T=0.542
PMID Title Author Journal
28440896Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.Yin XAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs17608034E-06nicotine dependence28440896

eQTL of rs1760803 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 rs1760803 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 )
chr1154296660154296754E06738766
chr1154307195154307856E06749301
chr1154277412154277934E06819518
chr1154306805154306865E06848911
chr1154306874154307180E06848980
chr1154307195154307856E06849301
chr1154307195154307856E06949301
chr1154246419154246476E070-11418
chr1154306805154306865E07148911
chr1154306874154307180E07148980
chr1154307195154307856E07149301
chr1154306874154307180E07248980
chr1154307195154307856E07249301
chr1154303294154303434E07345400
chr1154307195154307856E07349301
chr1154306805154306865E07448911
chr1154306874154307180E07448980
chr1154307195154307856E07449301
chr1154244110154244164E081-13730
chr1154244261154244356E081-13538









Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1154244441154245596E067-12298
chr1154296837154300496E06738943
chr1154244441154245596E068-12298
chr1154296837154300496E06838943
chr1154244441154245596E069-12298
chr1154296837154300496E06938943
chr1154244441154245596E070-12298
chr1154296837154300496E07038943
chr1154244441154245596E071-12298
chr1154296837154300496E07138943
chr1154244441154245596E072-12298
chr1154296837154300496E07238943
chr1154244441154245596E073-12298
chr1154296837154300496E07338943
chr1154244441154245596E074-12298
chr1154296837154300496E07438943
chr1154244441154245596E081-12298
chr1154244441154245596E082-12298
chr1154296837154300496E08238943