rs10813367

Homo sapiens
G>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0396 (11827/29862,GnomAD)
T=0378 (11014/29118,TOPMED)
T=0371 (1859/5008,1000G)
T=0450 (1734/3854,ALSPAC)
T=0450 (1669/3708,TWINSUK)
chr9:30837983 (GRCh38.p7) (9p21.1)
CD
GWASdb2
1   publication(s)
See rs on genome
1 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.30837983G>T
GRCh37.p13 chr 9NC_000009.11:g.30837981G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.721T=0.279
1000GenomesAmericanSub694G=0.570T=0.430
1000GenomesEast AsianSub1008G=0.609T=0.391
1000GenomesEuropeSub1006G=0.498T=0.502
1000GenomesGlobalStudy-wide5008G=0.629T=0.371
1000GenomesSouth AsianSub978G=0.700T=0.300
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.550T=0.450
The Genome Aggregation DatabaseAfricanSub8708G=0.702T=0.298
The Genome Aggregation DatabaseAmericanSub830G=0.580T=0.420
The Genome Aggregation DatabaseEast AsianSub1612G=0.628T=0.372
The Genome Aggregation DatabaseEuropeSub18410G=0.557T=0.442
The Genome Aggregation DatabaseGlobalStudy-wide29862G=0.603T=0.396
The Genome Aggregation DatabaseOtherSub302G=0.530T=0.470
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.621T=0.378
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.550T=0.450
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
rs108133670.000136cocaine dependence23958962
rs108133670.000763cocaine dependence23958962

eQTL of rs10813367 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 rs10813367 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 )
chr93084677730846940E0688796