rs8082814

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0036 (1091/29978,GnomAD)
A=0041 (207/5008,1000G)
A=0000 (0/3854,ALSPAC)
A=0000 (1/3708,TWINSUK)
chr18:48450704 (GRCh38.p7) (18q21.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.48450704G>A
GRCh38.p7 chr 18NC_000018.10:g.48450704G>T
GRCh37.p13 chr 18NC_000018.9:g.45977075G>A
GRCh37.p13 chr 18NC_000018.9:g.45977075G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.852A=0.148
1000GenomesAmericanSub694G=0.980A=0.020
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=1.000A=0.000
1000GenomesGlobalStudy-wide5008G=0.959A=0.041
1000GenomesSouth AsianSub978G=1.000A=0.000
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=1.000A=0.000
The Genome Aggregation DatabaseAfricanSub8720G=0.875T=0.001
The Genome Aggregation DatabaseAmericanSub838G=1.000T=0.00,
The Genome Aggregation DatabaseEast AsianSub1618G=1.000T=0.000
The Genome Aggregation DatabaseEuropeSub18500G=0.999T=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29978G=0.963T=0.000
The Genome Aggregation DatabaseOtherSub302G=1.000T=0.00,
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=1.000A=0.000
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs80828140.000756alcohol dependence21314694

eQTL of rs8082814 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 rs8082814 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.