rs11944332

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0108 (3236/29954,GnomAD)
G=0113 (3289/29118,TOPMED)
G=0091 (457/5008,1000G)
G=0136 (526/3854,ALSPAC)
G=0145 (538/3708,TWINSUK)
chr4:173633681 (GRCh38.p7) (4q34.1)
CD
GWASdb2 | GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.173633681A>G
GRCh37.p13 chr 4NC_000004.11:g.174554832A>G
RANP6 pseudogeneNG_022039.2:g.835T>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.901G=0.099
1000GenomesAmericanSub694A=0.920G=0.080
1000GenomesEast AsianSub1008A=0.995G=0.005
1000GenomesEuropeSub1006A=0.861G=0.139
1000GenomesGlobalStudy-wide5008A=0.909G=0.091
1000GenomesSouth AsianSub978A=0.870G=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.864G=0.136
The Genome Aggregation DatabaseAfricanSub8726A=0.906G=0.094
The Genome Aggregation DatabaseAmericanSub838A=0.920G=0.080
The Genome Aggregation DatabaseEast AsianSub1622A=0.993G=0.007
The Genome Aggregation DatabaseEuropeSub18466A=0.875G=0.124
The Genome Aggregation DatabaseGlobalStudy-wide29954A=0.892G=0.108
The Genome Aggregation DatabaseOtherSub302A=0.890G=0.110
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.887G=0.113
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.855G=0.145
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
rs119443322E-06cocaine dependence23958962

eQTL of rs11944332 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 rs11944332 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.