rs12858772

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0286 (5891/20548,GnomAD)
T=0272 (1025/3775,1000G)
T=0242 (899/3708,TWINSUK)
T=0246 (711/2889,ALSPAC)
chrX:117353885 (GRCh38.p7) (Xq23)
AD
GWASdb2
1   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.117353885C>T
GRCh37.p13 chr XNC_000023.10:g.116487848C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1003C=0.529T=0.471
1000GenomesAmericanSub524C=0.850T=0.150
1000GenomesEast AsianSub764C=0.840T=0.160
1000GenomesEuropeSub766C=0.780T=0.220
1000GenomesGlobalStudy-wide3775C=0.728T=0.272
1000GenomesSouth AsianSub718C=0.740T=0.260
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide2889C=0.754T=0.246
The Genome Aggregation DatabaseAfricanSub5789C=0.555T=0.445
The Genome Aggregation DatabaseAmericanSub603C=0.850T=0.150
The Genome Aggregation DatabaseEast AsianSub1008C=0.853T=0.147
The Genome Aggregation DatabaseEuropeSub12965C=0.765T=0.234
The Genome Aggregation DatabaseGlobalStudy-wide20548C=0.713T=0.286
The Genome Aggregation DatabaseOtherSub183C=0.790T=0.210
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.758T=0.242
PMID Title Author Journal
19581569Genome-wide association study of alcohol dependence.Treutlein JArch Gen Psychiatry

P-Value

SNP ID p-value Traits Study
rs128587722.57E-06alcohol dependence19581569

eQTL of rs12858772 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 rs12858772 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.