rs10259781

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0096 (2892/29960,GnomAD)
A=0105 (3077/29118,TOPMED)
A=0086 (429/5008,1000G)
A=0056 (214/3854,ALSPAC)
A=0070 (258/3708,TWINSUK)
chr7:153169940 (GRCh38.p7) (7q36.2)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.153169940G>A
GRCh37.p13 chr 7NC_000007.13:g.152867025G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.805A=0.195
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=0.997A=0.003
1000GenomesEuropeSub1006G=0.932A=0.068
1000GenomesGlobalStudy-wide5008G=0.914A=0.086
1000GenomesSouth AsianSub978G=0.940A=0.060
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.944A=0.056
The Genome Aggregation DatabaseAfricanSub8710G=0.818A=0.182
The Genome Aggregation DatabaseAmericanSub838G=0.950A=0.050
The Genome Aggregation DatabaseEast AsianSub1620G=0.997A=0.003
The Genome Aggregation DatabaseEuropeSub18492G=0.932A=0.067
The Genome Aggregation DatabaseGlobalStudy-wide29960G=0.903A=0.096
The Genome Aggregation DatabaseOtherSub300G=0.960A=0.040
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.894A=0.105
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.930A=0.070
PMID Title Author Journal
23953852Genome-wide association studies of maximum number of drinks.Pan YJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs102597816.95E-05alcohol consumption23953852

eQTL of rs10259781 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 rs10259781 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.