rs932026

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0126 (3771/29940,GnomAD)
A=0166 (4848/29118,TOPMED)
A=0190 (954/5008,1000G)
A=0092 (355/3854,ALSPAC)
A=0092 (342/3708,TWINSUK)
chr18:38425547 (GRCh38.p7) (18q12.2)
AD
GWASdb2
2   publication(s)
See rs on genome
18 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.38425547G>A
GRCh37.p13 chr 18NC_000018.9:g.36005511G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.727A=0.273
1000GenomesAmericanSub694G=0.860A=0.140
1000GenomesEast AsianSub1008G=0.818A=0.182
1000GenomesEuropeSub1006G=0.894A=0.106
1000GenomesGlobalStudy-wide5008G=0.810A=0.190
1000GenomesSouth AsianSub978G=0.790A=0.210
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.908A=0.092
The Genome Aggregation DatabaseAfricanSub8704G=0.761A=0.239
The Genome Aggregation DatabaseAmericanSub838G=0.870A=0.130
The Genome Aggregation DatabaseEast AsianSub1612G=0.818A=0.182
The Genome Aggregation DatabaseEuropeSub18484G=0.931A=0.068
The Genome Aggregation DatabaseGlobalStudy-wide29940G=0.874A=0.126
The Genome Aggregation DatabaseOtherSub302G=0.900A=0.100
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.833A=0.166
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.908A=0.092
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res
22843504Individual common variants exert weak effects on the risk for autism spectrum disorders.Anney RHum Mol Genet

P-Value

SNP ID p-value Traits Study
rs9320260.000966alcohol dependence20201924

eQTL of rs932026 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 rs932026 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 )
chr183603838236038485E06932871
chr183603856436038719E06933053
chr183603876236038977E06933251
chr183603901936039809E06933508
chr183600080736001059E070-4452
chr183600106636001264E070-4247
chr183600128636001390E070-4121
chr183600193936002129E070-3382
chr183603901936039809E07033508
chr183603876236038977E07133251
chr183603856436038719E08133053
chr183603876236038977E08133251
chr183603901936039809E08133508
chr183600063536000689E082-4822
chr183600080736001059E082-4452
chr183600106636001264E082-4247
chr183600128636001390E082-4121
chr183603901936039809E08233508