rs17053982

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0092 (2771/29944,GnomAD)
A=0100 (2924/29118,TOPMED)
A=0105 (525/5008,1000G)
A=0061 (234/3854,ALSPAC)
A=0066 (245/3708,TWINSUK)
chr5:156861811 (GRCh38.p7) (5q33.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.156861811G>A
GRCh37.p13 chr 5NC_000005.9:g.156288822G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.885A=0.115
1000GenomesAmericanSub694G=0.920A=0.080
1000GenomesEast AsianSub1008G=0.893A=0.107
1000GenomesEuropeSub1006G=0.933A=0.067
1000GenomesGlobalStudy-wide5008G=0.895A=0.105
1000GenomesSouth AsianSub978G=0.850A=0.150
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.939A=0.061
The Genome Aggregation DatabaseAfricanSub8710G=0.880A=0.120
The Genome Aggregation DatabaseAmericanSub836G=0.920A=0.080
The Genome Aggregation DatabaseEast AsianSub1618G=0.894A=0.106
The Genome Aggregation DatabaseEuropeSub18478G=0.920A=0.079
The Genome Aggregation DatabaseGlobalStudy-wide29944G=0.907A=0.092
The Genome Aggregation DatabaseOtherSub302G=0.930A=0.070
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.899A=0.100
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.934A=0.066
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
rs170539820.000733alcohol dependence21314694

eQTL of rs17053982 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 rs17053982 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.