SNP Detail Info-rs618453

Organism: Homo sapiens

Alleles: A>G / A>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0389 (11660/29924,GnomAD)
A==0484 (14098/29118,TOPMED)
G=0384 (1925/5008,1000G)

Position: chr11:106362367 (GRCh38.p7) (11q22.3)

Phenotype: ND

Dataset:

GWASdb2

Publications: 1 publication(s)

Genomic View: See rs on genome

Enhancer: 0 Enhancer around

Promoter: 0 Promoter around

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	A=0.086	G=0.914
1000Genomes	American	Sub	694	A=0.770	G=0.230
1000Genomes	East Asian	Sub	1008	A=0.885	G=0.115
1000Genomes	Europe	Sub	1006	A=0.745	G=0.255
1000Genomes	Global	Study-wide	5008	A=0.616	G=0.384
1000Genomes	South Asian	Sub	978	A=0.810	G=0.190
The Genome Aggregation Database	African	Sub	8704	A=0.183	G=0.817
The Genome Aggregation Database	American	Sub	838	A=0.770	G=0.230
The Genome Aggregation Database	East Asian	Sub	1618	A=0.894	G=0.106
The Genome Aggregation Database	Europe	Sub	18464	A=0.778	G=0.221
The Genome Aggregation Database	Global	Study-wide	29924	A=0.610	G=0.389
The Genome Aggregation Database	Other	Sub	300	A=0.700	G=0.300
Trans-Omics for Precision Medicine	Global	Study-wide	29118	A=0.484	G=0.515

PMID	Title	Author	Journal
20158304	A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.	Lind PA	Twin Res Hum Genet

SNP ID	p-value	Traits	Study
rs618453	2.11E-05	alcohol and nictotine co-dependence	20158304

Position (v37)	eGene	GeneID	Variant	p-value	TSS	Tissue
There is no eQTL annotation for this SNP

Probe ID	Position	Gene	beta	p-value
There is no meQTL annotation for this SNP

rs618453