rs59551326

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0102 (3070/29988,GnomAD)
G=0104 (3041/29118,TOPMED)
G=0071 (356/5008,1000G)
G=0094 (363/3854,ALSPAC)
G=0098 (364/3708,TWINSUK)
chr21:25384656 (GRCh38.p7) (21q21.2)
AD
GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 21NC_000021.9:g.25384656A>G
GRCh37.p13 chr 21NC_000021.8:g.26756969A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.874G=0.126
1000GenomesAmericanSub694A=0.960G=0.040
1000GenomesEast AsianSub1008A=0.984G=0.016
1000GenomesEuropeSub1006A=0.909G=0.091
1000GenomesGlobalStudy-wide5008A=0.929G=0.071
1000GenomesSouth AsianSub978A=0.950G=0.050
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.906G=0.094
The Genome Aggregation DatabaseAfricanSub8728A=0.857G=0.143
The Genome Aggregation DatabaseAmericanSub836A=0.970G=0.030
The Genome Aggregation DatabaseEast AsianSub1622A=0.967G=0.033
The Genome Aggregation DatabaseEuropeSub18500A=0.906G=0.093
The Genome Aggregation DatabaseGlobalStudy-wide29988A=0.897G=0.102
The Genome Aggregation DatabaseOtherSub302A=0.940G=0.060
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.895G=0.104
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.902G=0.098
PMID Title Author Journal
24166409Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.Gelernter JMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs595513269.00E-07alcohol dependence24166409
rs595513265.00E-06alcohol dependence24166409

eQTL of rs59551326 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 rs59551326 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.