rs4758405

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0491 (14692/29914,GnomAD)
G==0480 (13981/29118,TOPMED)
A=0475 (2378/5008,1000G)
A=0412 (1588/3854,ALSPAC)
A=0422 (1564/3708,TWINSUK)
chr11:6303404 (GRCh38.p7) (11p15.4)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 11NC_000011.10:g.6303404G>A
GRCh38.p7 chr 11NC_000011.10:g.6303404G>T
GRCh37.p13 chr 11NC_000011.9:g.6324634G>A
GRCh37.p13 chr 11NC_000011.9:g.6324634G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.373A=0.627
1000GenomesAmericanSub694G=0.520A=0.480
1000GenomesEast AsianSub1008G=0.570A=0.430
1000GenomesEuropeSub1006G=0.550A=0.450
1000GenomesGlobalStudy-wide5008G=0.525A=0.475
1000GenomesSouth AsianSub978G=0.660A=0.340
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.588A=0.412
The Genome Aggregation DatabaseAfricanSub8706G=0.389A=0.611
The Genome Aggregation DatabaseAmericanSub836G=0.500A=0.500
The Genome Aggregation DatabaseEast AsianSub1616G=0.592A=0.408
The Genome Aggregation DatabaseEuropeSub18454G=0.560A=0.439
The Genome Aggregation DatabaseGlobalStudy-wide29914G=0.508A=0.491
The Genome Aggregation DatabaseOtherSub302G=0.390A=0.610
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.480A=0.519
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.578A=0.422
PMID Title Author Journal
19268276Genome-wide association study of smoking initiation and current smoking.Vink JMAm J Hum Genet

P-Value

SNP ID p-value Traits Study
rs47584058.41E-06nicotine smoking19268276

eQTL of rs4758405 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 rs4758405 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.