rs4440177

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0445 (13325/29890,GnomAD)
G==0479 (13954/29118,TOPMED)
A=0494 (2475/5008,1000G)
A=0333 (1282/3854,ALSPAC)
A=0334 (1239/3708,TWINSUK)
chr4:162321901 (GRCh38.p7) (4q32.2)
ND | AD
GWASdb2 | GWASCatalog
1   publication(s)
See rs on genome
4 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.162321901G>A
GRCh37.p13 chr 4NC_000004.11:g.163243053G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.267A=0.733
1000GenomesAmericanSub694G=0.580A=0.420
1000GenomesEast AsianSub1008G=0.558A=0.442
1000GenomesEuropeSub1006G=0.654A=0.346
1000GenomesGlobalStudy-wide5008G=0.506A=0.494
1000GenomesSouth AsianSub978G=0.570A=0.430
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.667A=0.333
The Genome Aggregation DatabaseAfricanSub8718G=0.313A=0.687
The Genome Aggregation DatabaseAmericanSub834G=0.540A=0.460
The Genome Aggregation DatabaseEast AsianSub1606G=0.567A=0.433
The Genome Aggregation DatabaseEuropeSub18430G=0.669A=0.330
The Genome Aggregation DatabaseGlobalStudy-wide29890G=0.554A=0.445
The Genome Aggregation DatabaseOtherSub302G=0.460A=0.540
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.479A=0.520
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.666A=0.334
PMID Title Author Journal
23942779A genome-wide association study of behavioral disinhibition.McGue MBehav Genet

P-Value

SNP ID p-value Traits Study
rs44401770.000006alcohol dependence23942779
rs44401770.00041nicotine use23942779
rs44401770.00066alcohol consumption23942779

eQTL of rs4440177 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 rs4440177 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 )
chr4163274008163274115E06730955
chr4163274008163274115E06930955
chr4163274008163274115E07430955
chr4163269035163269270E08125982