rs10064702

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0392 (11723/29836,GnomAD)
G=0423 (12331/29118,TOPMED)
G=0413 (2069/5008,1000G)
G=0364 (1401/3854,ALSPAC)
G=0362 (1344/3708,TWINSUK)
chr5:50336928 (GRCh38.p7) (5q11.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.50336928T>G
GRCh37.p13 chr 5NC_000005.9:g.49632762T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.486G=0.514
1000GenomesAmericanSub694T=0.670G=0.330
1000GenomesEast AsianSub1008T=0.526G=0.474
1000GenomesEuropeSub1006T=0.669G=0.331
1000GenomesGlobalStudy-wide5008T=0.587G=0.413
1000GenomesSouth AsianSub978T=0.640G=0.360
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.636G=0.364
The Genome Aggregation DatabaseAfricanSub8684T=0.477G=0.523
The Genome Aggregation DatabaseAmericanSub836T=0.660G=0.340
The Genome Aggregation DatabaseEast AsianSub1582T=0.485G=0.515
The Genome Aggregation DatabaseEuropeSub18432T=0.675G=0.324
The Genome Aggregation DatabaseGlobalStudy-wide29836T=0.607G=0.392
The Genome Aggregation DatabaseOtherSub302T=0.680G=0.320
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.576G=0.423
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.638G=0.362
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs100647020.0000915alcoholismpha002891
rs100647020.0000915alcohol dependence20201924

eQTL of rs10064702 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 rs10064702 in Fetal Brain

Probe ID Position Gene beta p-value
cg15950743chr5:49708521EMB-0.088830637498681.0654e-35

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.