rs7645282

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0200 (5992/29846,GnomAD)
G=0282 (8216/29118,TOPMED)
G=0221 (1106/5008,1000G)
G=0104 (401/3854,ALSPAC)
G=0108 (399/3708,TWINSUK)
chr3:164842394 (GRCh38.p7) (3q26.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.164842394A>G
GRCh37.p13 chr 3NC_000003.11:g.164560182A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.458G=0.542
1000GenomesAmericanSub694A=0.900G=0.100
1000GenomesEast AsianSub1008A=0.902G=0.098
1000GenomesEuropeSub1006A=0.907G=0.093
1000GenomesGlobalStudy-wide5008A=0.779G=0.221
1000GenomesSouth AsianSub978A=0.870G=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.896G=0.104
The Genome Aggregation DatabaseAfricanSub8638A=0.525G=0.475
The Genome Aggregation DatabaseAmericanSub832A=0.930G=0.070
The Genome Aggregation DatabaseEast AsianSub1608A=0.891G=0.109
The Genome Aggregation DatabaseEuropeSub18466A=0.911G=0.088
The Genome Aggregation DatabaseGlobalStudy-wide29846A=0.799G=0.200
The Genome Aggregation DatabaseOtherSub302A=0.910G=0.090
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.717G=0.282
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.892G=0.108
PMID Title Author Journal
24962325Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.Kapoor MDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs76452822.07E-08alcohol dependence (age at onset)24962325

eQTL of rs7645282 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 rs7645282 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.