rs16894266

Homo sapiens
A>G
LOC105374693 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0038 (1152/29956,GnomAD)
G=0052 (1530/29118,TOPMED)
G=0048 (241/5008,1000G)
G=0002 (7/3854,ALSPAC)
G=0002 (9/3708,TWINSUK)
chr5:25258761 (GRCh38.p7) (5p14.1)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.25258761A>G
GRCh37.p13 chr 5NC_000005.9:g.25258870A>G

Gene: LOC105374693, uncharacterized LOC105374693(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LINC02211 transcriptNR_136209.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.860G=0.140
1000GenomesAmericanSub694A=0.980G=0.020
1000GenomesEast AsianSub1008A=0.999G=0.001
1000GenomesEuropeSub1006A=0.997G=0.003
1000GenomesGlobalStudy-wide5008A=0.952G=0.048
1000GenomesSouth AsianSub978A=0.960G=0.040
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.998G=0.002
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.947G=0.052
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.998G=0.002
PMID Title Author Journal
17158188Novel genes identified in a high-density genome wide association study for nicotine dependence.Bierut LJHum Mol Genet

P-Value

SNP ID p-value Traits Study
rs168942660.000903nicotine dependence17158188

eQTL of rs16894266 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 rs16894266 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.