rs7532171

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0136 (4088/29960,GnomAD)
T=0125 (3665/29118,TOPMED)
T=0180 (901/5008,1000G)
T=0083 (320/3854,ALSPAC)
T=0095 (353/3708,TWINSUK)
chr1:101259395 (GRCh38.p7) (1p21.2)
ND
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.101259395C>T
GRCh37.p13 chr 1NC_000001.10:g.101724951C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.846T=0.154
1000GenomesAmericanSub694C=0.880T=0.120
1000GenomesEast AsianSub1008C=0.571T=0.429
1000GenomesEuropeSub1006C=0.884T=0.116
1000GenomesGlobalStudy-wide5008C=0.820T=0.180
1000GenomesSouth AsianSub978C=0.940T=0.060
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.917T=0.083
The Genome Aggregation DatabaseAfricanSub8712C=0.844T=0.156
The Genome Aggregation DatabaseAmericanSub836C=0.840T=0.160
The Genome Aggregation DatabaseEast AsianSub1608C=0.602T=0.398
The Genome Aggregation DatabaseEuropeSub18502C=0.896T=0.103
The Genome Aggregation DatabaseGlobalStudy-wide29960C=0.863T=0.136
The Genome Aggregation DatabaseOtherSub302C=0.900T=0.100
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.874T=0.125
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.905T=0.095
PMID Title Author Journal
20158304A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.Lind PATwin Res Hum Genet

P-Value

SNP ID p-value Traits Study
rs75321713.81E-05alcohol and nictotine co-dependence20158304

eQTL of rs7532171 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 rs7532171 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 )
chr1101756040101756631E06831089
chr1101756673101756777E06831722
chr1101728583101728713E0693632
chr1101682895101682975E070-41976
chr1101684909101685089E070-39862
chr1101685204101685262E070-39689
chr1101685582101685813E070-39138
chr1101685895101686150E070-38801
chr1101749060101749302E07024109
chr1101723944101724056E071-895
chr1101727751101727877E0712800
chr1101753708101754529E07128757
chr1101757056101757555E07132105
chr1101757581101757703E07132630
chr1101753708101754529E07228757
chr1101728583101728713E0743632
chr1101685204101685262E081-39689
chr1101685582101685813E081-39138
chr1101685895101686150E081-38801







Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1101700692101703534E067-21417
chr1101703586101705585E067-19366
chr1101705618101706118E067-18833
chr1101706187101706324E067-18627
chr1101700692101703534E068-21417
chr1101703586101705585E068-19366
chr1101705618101706118E068-18833
chr1101706187101706324E068-18627
chr1101706363101706411E068-18540
chr1101700692101703534E069-21417
chr1101703586101705585E069-19366
chr1101703586101705585E070-19366
chr1101705618101706118E070-18833
chr1101706187101706324E070-18627
chr1101706363101706411E070-18540
chr1101700692101703534E071-21417
chr1101703586101705585E071-19366
chr1101705618101706118E071-18833
chr1101706187101706324E071-18627
chr1101706363101706411E071-18540
chr1101700692101703534E072-21417
chr1101703586101705585E072-19366
chr1101700692101703534E073-21417
chr1101703586101705585E073-19366
chr1101705618101706118E073-18833
chr1101700692101703534E074-21417
chr1101703586101705585E074-19366
chr1101705618101706118E074-18833
chr1101706187101706324E074-18627
chr1101706363101706411E074-18540
chr1101700692101703534E082-21417
chr1101703586101705585E082-19366
chr1101705618101706118E082-18833
chr1101706187101706324E082-18627