SNP Detail Info-rs11636705

Organism: Homo sapiens

Alleles: C>A / C>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

T=0153 (4589/29952,GnomAD)
T=0144 (4211/29118,TOPMED)
T=0160 (803/5008,1000G)
T=0165 (635/3854,ALSPAC)
T=0153 (568/3708,TWINSUK)

Position: chr15:96062683 (GRCh38.p7) (15q26.2)

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	C=0.852	T=0.148
1000Genomes	American	Sub	694	C=0.820	T=0.180
1000Genomes	East Asian	Sub	1008	C=0.898	T=0.102
1000Genomes	Europe	Sub	1006	C=0.843	T=0.157
1000Genomes	Global	Study-wide	5008	C=0.840	T=0.160
1000Genomes	South Asian	Sub	978	C=0.770	T=0.230
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.835	T=0.165
The Genome Aggregation Database	African	Sub	8726	C=0.853	T=0.147
The Genome Aggregation Database	American	Sub	838	C=0.820	T=0.18,
The Genome Aggregation Database	East Asian	Sub	1618	C=0.902	T=0.097
The Genome Aggregation Database	Europe	Sub	18468	C=0.840	T=0.159
The Genome Aggregation Database	Global	Study-wide	29952	C=0.846	T=0.153
The Genome Aggregation Database	Other	Sub	302	C=0.810	T=0.19,
Trans-Omics for Precision Medicine	Global	Study-wide	29118	C=0.855	T=0.144
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.847	T=0.153

PMID	Title	Author	Journal
19268276	Genome-wide association study of smoking initiation and current smoking.	Vink JM	Am J Hum Genet

SNP ID	p-value	Traits	Study
rs11636705	5.39E-05	nicotine smoking	19268276

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

rs11636705