rs16843093

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0095 (2853/29874,GnomAD)
G=0120 (3515/29118,TOPMED)
G=0146 (732/5008,1000G)
G=0034 (132/3854,ALSPAC)
G=0030 (112/3708,TWINSUK)
chr1:198447545 (GRCh38.p7) (1q31.3)
ND
GWASdb2
1   publication(s)
See rs on genome
4 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.198447545A>G
GRCh37.p13 chr 1NC_000001.10:g.198416675A>G
GRCh38.p7 chr 1 alt locus HSCHR1_3_CTG31NW_003315907.2:g.77463A>G
GRCh37.p13 chr 1 novel patch HSCHR1_3_CTG31NW_003315907.1:g.77463A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.759G=0.241
1000GenomesAmericanSub694A=0.860G=0.140
1000GenomesEast AsianSub1008A=0.825G=0.175
1000GenomesEuropeSub1006A=0.963G=0.037
1000GenomesGlobalStudy-wide5008A=0.854G=0.146
1000GenomesSouth AsianSub978A=0.890G=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.966G=0.034
The Genome Aggregation DatabaseAfricanSub8702A=0.811G=0.189
The Genome Aggregation DatabaseAmericanSub830A=0.800G=0.200
The Genome Aggregation DatabaseEast AsianSub1608A=0.823G=0.177
The Genome Aggregation DatabaseEuropeSub18432A=0.959G=0.040
The Genome Aggregation DatabaseGlobalStudy-wide29874A=0.904G=0.095
The Genome Aggregation DatabaseOtherSub302A=0.970G=0.030
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.879G=0.120
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.970G=0.030
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
rs168430930.000164nicotine dependence17158188

eQTL of rs16843093 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 rs16843093 in Fetal Brain

Probe ID Position Gene beta p-value
cg17942929chr17:43168803NMT1-0.0395088229471191.0219e-9

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr1198460280198461019E06743605
chr1198450793198451297E07134118
chr1198466247198466315E08149572
chr1198466387198466659E08149712