rs4525572

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0477 (14259/29888,GnomAD)
G=0408 (11887/29118,TOPMED)
G=0344 (1721/5008,1000G)
A==0409 (1578/3854,ALSPAC)
A==0399 (1480/3708,TWINSUK)
chr18:27836281 (GRCh38.p7) (18q12.1)
CD
GWASdb2
1   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.27836281A>G
GRCh37.p13 chr 18NC_000018.9:g.25416245A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.877G=0.123
1000GenomesAmericanSub694A=0.450G=0.550
1000GenomesEast AsianSub1008A=0.755G=0.245
1000GenomesEuropeSub1006A=0.411G=0.589
1000GenomesGlobalStudy-wide5008A=0.656G=0.344
1000GenomesSouth AsianSub978A=0.660G=0.340
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.409G=0.591
The Genome Aggregation DatabaseAfricanSub8714A=0.788G=0.212
The Genome Aggregation DatabaseAmericanSub836A=0.500G=0.500
The Genome Aggregation DatabaseEast AsianSub1596A=0.764G=0.236
The Genome Aggregation DatabaseEuropeSub18440A=0.380G=0.619
The Genome Aggregation DatabaseGlobalStudy-wide29888A=0.522G=0.477
The Genome Aggregation DatabaseOtherSub302A=0.390G=0.610
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.591G=0.408
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.399G=0.601
PMID Title Author Journal
23958962Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.Gelernter JMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs45255720.0000642cocaine dependence23958962
rs45255720.000163cocaine dependence23958962

eQTL of rs4525572 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 rs4525572 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.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr182540495625405047E070-11198
chr182540513025405488E070-10757
chr182540549525405622E070-10623
chr182540569225405766E070-10479
chr182540583625406010E070-10235
chr182541203925412300E070-3945