rs4285401

Homo sapiens
A>G
LOC102723686 : 2KB Upstream Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0410 (12267/29908,GnomAD)
G=0353 (10281/29118,TOPMED)
G=0324 (1621/5008,1000G)
A==0433 (1670/3854,ALSPAC)
A==0443 (1641/3708,TWINSUK)
chr7:153181248 (GRCh38.p7) (7q36.2)
ND
GWASdb2 | GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.153181248A>G
GRCh37.p13 chr 7NC_000007.13:g.152878333A>G

Gene: LOC102723686, uncharacterized LOC102723686(plus strand): 2KB Upstream Variant

Molecule type Change Amino acid[Codon] SO Term
LOC102723686 transcriptXR_001745433.1:n.N/AUpstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.901G=0.099
1000GenomesAmericanSub694A=0.660G=0.340
1000GenomesEast AsianSub1008A=0.743G=0.257
1000GenomesEuropeSub1006A=0.464G=0.536
1000GenomesGlobalStudy-wide5008A=0.676G=0.324
1000GenomesSouth AsianSub978A=0.540G=0.460
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.433G=0.567
The Genome Aggregation DatabaseAfricanSub8708A=0.839G=0.161
The Genome Aggregation DatabaseAmericanSub836A=0.650G=0.350
The Genome Aggregation DatabaseEast AsianSub1616A=0.770G=0.230
The Genome Aggregation DatabaseEuropeSub18446A=0.455G=0.544
The Genome Aggregation DatabaseGlobalStudy-wide29908A=0.589G=0.410
The Genome Aggregation DatabaseOtherSub302A=0.490G=0.510
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.646G=0.353
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.443G=0.557
PMID Title Author Journal
23942779A genome-wide association study of behavioral disinhibition.McGue MBehav Genet

P-Value

SNP ID p-value Traits Study
rs42854012E-06nicotine use23942779

eQTL of rs4285401 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 rs4285401 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.