rs1868152

Homo sapiens
A>G / A>T
None
Check p-value
SNV (Single Nucleotide Variation)
A==0144 (4328/29932,GnomAD)
A==0157 (4575/29118,TOPMED)
A==0144 (723/5008,1000G)
A==0129 (496/3854,ALSPAC)
A==0135 (502/3708,TWINSUK)
chr3:186502274 (GRCh38.p7) (3q27.3)
AD | ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.186502274A>G
GRCh38.p7 chr 3NC_000003.12:g.186502274A>T
GRCh37.p13 chr 3NC_000003.11:g.186220063A>G
GRCh37.p13 chr 3NC_000003.11:g.186220063A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.225G=0.775
1000GenomesAmericanSub694A=0.130G=0.870
1000GenomesEast AsianSub1008A=0.086G=0.914
1000GenomesEuropeSub1006A=0.119G=0.881
1000GenomesGlobalStudy-wide5008A=0.144G=0.856
1000GenomesSouth AsianSub978A=0.130G=0.870
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.129G=0.871
The Genome Aggregation DatabaseAfricanSub8694A=0.210G=0.790
The Genome Aggregation DatabaseAmericanSub838A=0.100G=0.900
The Genome Aggregation DatabaseEast AsianSub1622A=0.062G=0.938
The Genome Aggregation DatabaseEuropeSub18476A=0.124G=0.875
The Genome Aggregation DatabaseGlobalStudy-wide29932A=0.144G=0.855
The Genome Aggregation DatabaseOtherSub302A=0.100G=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.157G=0.842
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.135G=0.865
PMID Title Author Journal
23942779A genome-wide association study of behavioral disinhibition.McGue MBehav Genet

P-Value

SNP ID p-value Traits Study
rs18681520.00022nicotine use23942779
rs18681520.0007alcohol consumption23942779

eQTL of rs1868152 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 rs1868152 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.