rs4610908

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0242 (5012/20715,GnomAD)
A=0198 (749/3775,1000G)
A=0245 (908/3708,TWINSUK)
A=0244 (704/2889,ALSPAC)
chrX:35166418 (GRCh38.p7) (Xp21.1)
AD | ND
GWASdb2
4   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr XNC_000023.11:g.35166418G>A
GRCh37.p13 chr XNC_000023.10:g.35184535G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1003G=0.713A=0.287
1000GenomesAmericanSub524G=0.850A=0.150
1000GenomesEast AsianSub764G=0.940A=0.060
1000GenomesEuropeSub766G=0.760A=0.240
1000GenomesGlobalStudy-wide3775G=0.802A=0.198
1000GenomesSouth AsianSub718G=0.790A=0.210
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide2889G=0.756A=0.244
The Genome Aggregation DatabaseAfricanSub5832G=0.725A=0.275
The Genome Aggregation DatabaseAmericanSub613G=0.890A=0.110
The Genome Aggregation DatabaseEast AsianSub1017G=0.936A=0.064
The Genome Aggregation DatabaseEuropeSub13069G=0.753A=0.246
The Genome Aggregation DatabaseGlobalStudy-wide20715G=0.758A=0.242
The Genome Aggregation DatabaseOtherSub184G=0.710A=0.290
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.755A=0.245
PMID Title Author Journal
22096494A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study.Zuo LPLoS One
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res
20202923A genome-wide association study of alcohol dependence.Bierut LJProc Natl Acad Sci U S A
22488850Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence.Zuo LAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs46109080.00000032alcohol and nictotine co-dependence22488850
rs46109080.00000057alcohol dependence22096494
rs46109080.00000549alcohol dependence20202923
rs46109080.000581alcohol dependence20201924

eQTL of rs4610908 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 rs4610908 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.