rs1779517

Homo sapiens
C>A / C>G
None
Check p-value
SNV (Single Nucleotide Variation)
C==0230 (6879/29904,GnomAD)
C==0213 (6218/29118,TOPMED)
C==0216 (1082/5008,1000G)
C==0279 (1076/3854,ALSPAC)
C==0277 (1026/3708,TWINSUK)
chr14:41261318 (GRCh38.p7) (14q21.1)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 14NC_000014.9:g.41261318C>A
GRCh38.p7 chr 14NC_000014.9:g.41261318C>G
GRCh37.p13 chr 14NC_000014.8:g.41730521C>A
GRCh37.p13 chr 14NC_000014.8:g.41730521C>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.114A=0.883
1000GenomesAmericanSub694C=0.210A=0.79,
1000GenomesEast AsianSub1008C=0.198A=0.802
1000GenomesEuropeSub1006C=0.262A=0.738
1000GenomesGlobalStudy-wide5008C=0.216A=0.783
1000GenomesSouth AsianSub978C=0.330A=0.67,
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.279A=0.721
The Genome Aggregation DatabaseAfricanSub8712C=0.169G=0.002
The Genome Aggregation DatabaseAmericanSub834C=0.170G=0.00,
The Genome Aggregation DatabaseEast AsianSub1610C=0.202G=0.000
The Genome Aggregation DatabaseEuropeSub18446C=0.263G=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29904C=0.230G=0.000
The Genome Aggregation DatabaseOtherSub302C=0.240G=0.00,
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.213A=0.786
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.277A=0.723
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
rs17795170.000112nicotine dependence17158188

eQTL of rs1779517 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 rs1779517 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.