rs4778700

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
A==0174 (5180/29730,GnomAD)
A==0161 (4708/29118,TOPMED)
A==0135 (678/5008,1000G)
A==0241 (930/3854,ALSPAC)
A==0226 (837/3708,TWINSUK)
chr15:79495493 (GRCh38.p7) (15q25.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 15NC_000015.10:g.79495493A>G
GRCh37.p13 chr 15NC_000015.9:g.79787835A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.072G=0.928
1000GenomesAmericanSub694A=0.170G=0.830
1000GenomesEast AsianSub1008A=0.069G=0.931
1000GenomesEuropeSub1006A=0.210G=0.790
1000GenomesGlobalStudy-wide5008A=0.135G=0.865
1000GenomesSouth AsianSub978A=0.190G=0.810
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.241G=0.759
The Genome Aggregation DatabaseAfricanSub8650A=0.090G=0.910
The Genome Aggregation DatabaseAmericanSub836A=0.140G=0.860
The Genome Aggregation DatabaseEast AsianSub1616A=0.092G=0.908
The Genome Aggregation DatabaseEuropeSub18328A=0.221G=0.778
The Genome Aggregation DatabaseGlobalStudy-wide29730A=0.174G=0.825
The Genome Aggregation DatabaseOtherSub300A=0.240G=0.760
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.161G=0.838
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.226G=0.774
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs47787000.000966alcohol dependence21314694

eQTL of rs4778700 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 rs4778700 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 )
chr157980580679806045E07017971
chr157980617079806224E07018335
chr157980642879806536E07018593
chr157980533879805712E08117503
chr157980580679806045E08117971
chr157980617079806224E08118335
chr157980642879806536E08118593
chr157980580679806045E08217971
chr157980617079806224E08218335
chr157980642879806536E08218593