rs11023571

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0349 (10433/29890,GnomAD)
A=0378 (11016/29118,TOPMED)
A=0356 (1783/5008,1000G)
A=0339 (1307/3854,ALSPAC)
A=0356 (1321/3708,TWINSUK)
chr11:15434922 (GRCh38.p7) (11p15.2)
AD
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 11NC_000011.10:g.15434922G>A
GRCh38.p7 chr 11NC_000011.10:g.15434922G>T
GRCh37.p13 chr 11NC_000011.9:g.15456468G>A
GRCh37.p13 chr 11NC_000011.9:g.15456468G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.640A=0.360
1000GenomesAmericanSub694G=0.570A=0.430
1000GenomesEast AsianSub1008G=0.770A=0.230
1000GenomesEuropeSub1006G=0.642A=0.358
1000GenomesGlobalStudy-wide5008G=0.644A=0.356
1000GenomesSouth AsianSub978G=0.570A=0.430
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.661A=0.339
The Genome Aggregation DatabaseAfricanSub8708G=0.633A=0.367
The Genome Aggregation DatabaseAmericanSub838G=0.560A=0.440
The Genome Aggregation DatabaseEast AsianSub1604G=0.787A=0.213
The Genome Aggregation DatabaseEuropeSub18440G=0.653A=0.346
The Genome Aggregation DatabaseGlobalStudy-wide29890G=0.651A=0.349
The Genome Aggregation DatabaseOtherSub300G=0.570A=0.430
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.621A=0.378
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.644A=0.356
PMID Title Author Journal
24277619ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample.Quillen EEAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs110235710.000879alcohol dependence24277619

eQTL of rs11023571 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 rs11023571 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 )
chr113157950031579943E069-18838
chr113158000231580124E069-18657
chr113158052531580575E069-18206
chr113163062831630682E07231847
chr113157950031579943E081-18838
chr113158000231580124E081-18657
chr113158052531580575E081-18206