rs4656703

Homo sapiens
A>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0301 (9012/29856,GnomAD)
C=0327 (9544/29118,TOPMED)
C=0375 (1879/5008,1000G)
C=0253 (974/3854,ALSPAC)
C=0241 (895/3708,TWINSUK)
chr1:169718994 (GRCh38.p7) (1q24.2)
AD
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around
7 Promoters around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.169718994A>C
GRCh37.p13 chr 1NC_000001.10:g.169688135A>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.571C=0.429
1000GenomesAmericanSub694A=0.640C=0.360
1000GenomesEast AsianSub1008A=0.671C=0.329
1000GenomesEuropeSub1006A=0.713C=0.287
1000GenomesGlobalStudy-wide5008A=0.625C=0.375
1000GenomesSouth AsianSub978A=0.550C=0.450
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.747C=0.253
The Genome Aggregation DatabaseAfricanSub8688A=0.615C=0.385
The Genome Aggregation DatabaseAmericanSub838A=0.600C=0.400
The Genome Aggregation DatabaseEast AsianSub1602A=0.656C=0.344
The Genome Aggregation DatabaseEuropeSub18426A=0.746C=0.253
The Genome Aggregation DatabaseGlobalStudy-wide29856A=0.698C=0.301
The Genome Aggregation DatabaseOtherSub302A=0.670C=0.330
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.672C=0.327
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.759C=0.241
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs46567030.0000448alcoholismpha002891
rs46567030.0000448alcohol dependence20201924

eQTL of rs4656703 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr1:169688135RN7SL333PENSG00000239494.2A>C3.6310e-3-140762Cerebellar_Hemisphere

meQTL of rs4656703 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.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr1169663053169664067E071-24068
chr1169664116169664389E071-23746
chr1169661474169662757E074-25378


Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1169680599169681493E067-6642
chr1169680599169681493E068-6642
chr1169680599169681493E069-6642
chr1169680599169681493E071-6642
chr1169680599169681493E072-6642
chr1169680599169681493E073-6642
chr1169680599169681493E074-6642