rs1328433

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
A==0308 (9226/29914,GnomAD)
A==0340 (9918/29118,TOPMED)
A==0249 (1246/5008,1000G)
A==0287 (1105/3854,ALSPAC)
A==0280 (1040/3708,TWINSUK)
chr9:80128905 (GRCh38.p7) (9q21.31)
AD
GWASdb2
1   publication(s)
See rs on genome
9 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.80128905A>G
GRCh37.p13 chr 9NC_000009.11:g.82743820A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.443G=0.557
1000GenomesAmericanSub694A=0.190G=0.810
1000GenomesEast AsianSub1008A=0.042G=0.958
1000GenomesEuropeSub1006A=0.280G=0.720
1000GenomesGlobalStudy-wide5008A=0.249G=0.751
1000GenomesSouth AsianSub978A=0.210G=0.790
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.287G=0.713
The Genome Aggregation DatabaseAfricanSub8702A=0.425G=0.575
The Genome Aggregation DatabaseAmericanSub832A=0.190G=0.810
The Genome Aggregation DatabaseEast AsianSub1616A=0.042G=0.958
The Genome Aggregation DatabaseEuropeSub18462A=0.281G=0.718
The Genome Aggregation DatabaseGlobalStudy-wide29914A=0.308G=0.691
The Genome Aggregation DatabaseOtherSub302A=0.330G=0.670
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.340G=0.659
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.280G=0.720
PMID Title Author Journal
21529783A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.Heath ACBiol Psychiatry

P-Value

SNP ID p-value Traits Study
rs13284335E-05alcoholism (heaviness of drinking)21529783

eQTL of rs1328433 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 rs1328433 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 )
chr98277356582774172E06829745
chr98277177482773115E07027954
chr98277316182773374E07029341
chr98277338882773483E07029568
chr98277356582774172E07029745
chr98277177482773115E08227954
chr98277316182773374E08229341
chr98277338882773483E08229568
chr98277356582774172E08229745