rs10759883

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
C==0424 (12690/29872,GnomAD)
C==0409 (11925/29118,TOPMED)
C==0445 (2229/5008,1000G)
C==0438 (1688/3854,ALSPAC)
C==0414 (1534/3708,TWINSUK)
chr9:95790481 (GRCh38.p7) (9q22.32)
ND
GWASCatalog
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.95790481C>T
GRCh37.p13 chr 9NC_000009.11:g.98552763C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.346T=0.654
1000GenomesAmericanSub694C=0.500T=0.500
1000GenomesEast AsianSub1008C=0.494T=0.506
1000GenomesEuropeSub1006C=0.420T=0.580
1000GenomesGlobalStudy-wide5008C=0.445T=0.555
1000GenomesSouth AsianSub978C=0.520T=0.480
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.438T=0.562
The Genome Aggregation DatabaseAfricanSub8704C=0.353T=0.647
The Genome Aggregation DatabaseAmericanSub838C=0.500T=0.500
The Genome Aggregation DatabaseEast AsianSub1612C=0.507T=0.493
The Genome Aggregation DatabaseEuropeSub18416C=0.447T=0.552
The Genome Aggregation DatabaseGlobalStudy-wide29872C=0.424T=0.575
The Genome Aggregation DatabaseOtherSub302C=0.470T=0.530
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.409T=0.590
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.414T=0.586
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
rs107598831E-06nicotine dependence28440896

eQTL of rs10759883 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr9:98552763LINC00476ENSG00000175611.7C>T4.6676e-10-85219Cerebellum
Chr9:98552763LINC00476ENSG00000175611.7C>T7.0049e-9-85219Frontal_Cortex_BA9
Chr9:98552763ERCC6L2ENSG00000182150.11C>T9.8594e-3-85497Frontal_Cortex_BA9
Chr9:98552763LINC00476ENSG00000175611.7C>T8.1594e-12-85219Hypothalamus
Chr9:98552763LINC00476ENSG00000175611.7C>T4.9980e-14-85219Cortex
Chr9:98552763LINC00476ENSG00000175611.7C>T1.6706e-14-85219Caudate_basal_ganglia
Chr9:98552763LINC00476ENSG00000175611.7C>T2.0424e-9-85219Brain_Spinal_cord_cervical
Chr9:98552763LINC00476ENSG00000175611.7C>T9.4609e-9-85219Hippocampus
Chr9:98552763LINC00476ENSG00000175611.7C>T4.0680e-5-85219Substantia_nigra
Chr9:98552763LINC00476ENSG00000175611.7C>T3.1868e-12-85219Putamen_basal_ganglia
Chr9:98552763LINC00476ENSG00000175611.7C>T1.7043e-12-85219Anterior_cingulate_cortex
Chr9:98552763LINC00476ENSG00000175611.7C>T1.5002e-8-85219Nucleus_accumbens_basal_ganglia
Chr9:98552763LINC00476ENSG00000175611.7C>T2.9765e-7-85219Amygdala

meQTL of rs10759883 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 )
chr99853371598534560E067-18203
chr99853460298535203E067-17560
chr99853531798535579E067-17184
chr99855025798550643E067-2120
chr99855075798551041E067-1722
chr99855104498551258E067-1505
chr99853460298535203E068-17560
chr99853531798535579E068-17184
chr99857009698570238E06817333
chr99851587098517702E069-35061
chr99853371598534560E069-18203
chr99853460298535203E069-17560
chr99856888898568938E06916125
chr99856897898569208E06916215
chr99853460298535203E070-17560
chr99851587098517702E071-35061
chr99852321498523553E071-29210
chr99852366498523770E071-28993
chr99853460298535203E071-17560
chr99857009698570238E07117333
chr99857026098570706E07117497
chr99857073798570896E07117974
chr99857092698571002E07118163
chr99851874798519891E072-32872
chr99851992898519978E072-32785
chr99853371598534560E072-18203
chr99853460298535203E072-17560
chr99853531798535579E072-17184
chr99857009698570238E07217333
chr99851529998515358E073-37405
chr99851547198515548E073-37215
chr99851564198515741E073-37022
chr99851587098517702E073-35061
chr99857009698570238E07317333
chr99857026098570706E07317497
chr99857073798570896E07317974
chr99857092698571002E07318163
chr99853371598534560E074-18203
chr99853460298535203E074-17560
chr99856874098568790E07415977
chr99853371598534560E081-18203
chr99853460298535203E081-17560
chr99853371598534560E082-18203