rs10464585

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0261 (7794/29854,GnomAD)
G=0235 (6863/29118,TOPMED)
G=0356 (1783/5008,1000G)
G=0242 (931/3854,ALSPAC)
G=0238 (881/3708,TWINSUK)
chr7:93806655 (GRCh38.p7) (7q21.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.93806655A>G
GRCh37.p13 chr 7NC_000007.13:g.93435967A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.837G=0.163
1000GenomesAmericanSub694A=0.620G=0.380
1000GenomesEast AsianSub1008A=0.374G=0.626
1000GenomesEuropeSub1006A=0.720G=0.280
1000GenomesGlobalStudy-wide5008A=0.644G=0.356
1000GenomesSouth AsianSub978A=0.600G=0.400
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.758G=0.242
The Genome Aggregation DatabaseAfricanSub8710A=0.819G=0.181
The Genome Aggregation DatabaseAmericanSub832A=0.560G=0.440
The Genome Aggregation DatabaseEast AsianSub1574A=0.374G=0.626
The Genome Aggregation DatabaseEuropeSub18440A=0.739G=0.260
The Genome Aggregation DatabaseGlobalStudy-wide29854A=0.738G=0.261
The Genome Aggregation DatabaseOtherSub298A=0.790G=0.210
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.764G=0.235
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.762G=0.238
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
rs104645856.41E-05alcohol consumption23953852

eQTL of rs10464585 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 rs10464585 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.