rs4525630

Homo sapiens
C>G / C>T
None
Check p-value
SNV (Single Nucleotide Variation)
C==0379 (11350/29880,GnomAD)
C==0387 (11291/29118,TOPMED)
C==0414 (2075/5008,1000G)
C==0336 (1296/3854,ALSPAC)
C==0355 (1317/3708,TWINSUK)
chr2:146752321 (GRCh38.p7) (2q22.3)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.146752321C>G
GRCh38.p7 chr 2NC_000002.12:g.146752321C>T
GRCh37.p13 chr 2NC_000002.11:g.147509889C>G
GRCh37.p13 chr 2NC_000002.11:g.147509889C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.388G=0.612
1000GenomesAmericanSub694C=0.530G=0.470
1000GenomesEast AsianSub1008C=0.400G=0.600
1000GenomesEuropeSub1006C=0.392G=0.608
1000GenomesGlobalStudy-wide5008C=0.414G=0.586
1000GenomesSouth AsianSub978C=0.410G=0.590
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.336G=0.664
The Genome Aggregation DatabaseAfricanSub8686C=0.388G=0.612
The Genome Aggregation DatabaseAmericanSub838C=0.510G=0.49,
The Genome Aggregation DatabaseEast AsianSub1604C=0.365G=0.635
The Genome Aggregation DatabaseEuropeSub18450C=0.368G=0.631
The Genome Aggregation DatabaseGlobalStudy-wide29880C=0.379G=0.620
The Genome Aggregation DatabaseOtherSub302C=0.560G=0.44,
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.387G=0.612
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.355G=0.645
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
rs45256300.000205nicotine dependence17158188

eQTL of rs4525630 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 rs4525630 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.