rs1542668

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
A==0271 (8093/29786,GnomAD)
A==0281 (8207/29116,TOPMED)
A==0231 (1157/5008,1000G)
A==0320 (1232/3854,ALSPAC)
A==0327 (1213/3708,TWINSUK)
chr14:42079709 (GRCh38.p7) (14q21.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 14NC_000014.9:g.42079709A>G
GRCh37.p13 chr 14NC_000014.8:g.42548912A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.233G=0.767
1000GenomesAmericanSub694A=0.240G=0.760
1000GenomesEast AsianSub1008A=0.057G=0.943
1000GenomesEuropeSub1006A=0.356G=0.644
1000GenomesGlobalStudy-wide5008A=0.231G=0.769
1000GenomesSouth AsianSub978A=0.270G=0.730
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.320G=0.680
The Genome Aggregation DatabaseAfricanSub8706A=0.252G=0.748
The Genome Aggregation DatabaseAmericanSub830A=0.210G=0.790
The Genome Aggregation DatabaseEast AsianSub1596A=0.083G=0.917
The Genome Aggregation DatabaseEuropeSub18352A=0.298G=0.701
The Genome Aggregation DatabaseGlobalStudy-wide29786A=0.271G=0.728
The Genome Aggregation DatabaseOtherSub302A=0.350G=0.650
Trans-Omics for Precision MedicineGlobalStudy-wide29116A=0.281G=0.718
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.327G=0.673
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
rs15426682.7E-05alcoholism (heaviness of drinking)21529783

eQTL of rs1542668 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 rs1542668 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.