rs2464786

Homo sapiens
G>A
LOC107985945 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0397 (11748/29524,GnomAD)
A=0426 (2135/5008,1000G)
A=0403 (1554/3854,ALSPAC)
A=0412 (1528/3708,TWINSUK)
chr2:129792562 (GRCh38.p7) (2q21.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.129792562G>A
GRCh37.p13 chr 2NC_000002.11:g.130550135G>A

Gene: LOC107985945, uncharacterized LOC107985945(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC107985945 transcriptXR_001739711.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.849A=0.151
1000GenomesAmericanSub694G=0.540A=0.460
1000GenomesEast AsianSub1008G=0.400A=0.600
1000GenomesEuropeSub1006G=0.558A=0.442
1000GenomesGlobalStudy-wide5008G=0.574A=0.426
1000GenomesSouth AsianSub978G=0.420A=0.580
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.597A=0.403
The Genome Aggregation DatabaseAfricanSub8304G=0.798A=0.202
The Genome Aggregation DatabaseAmericanSub836G=0.530A=0.470
The Genome Aggregation DatabaseEast AsianSub1616G=0.437A=0.563
The Genome Aggregation DatabaseEuropeSub18466G=0.532A=0.467
The Genome Aggregation DatabaseGlobalStudy-wide29524G=0.602A=0.397
The Genome Aggregation DatabaseOtherSub302G=0.540A=0.460
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.588A=0.412
PMID Title Author Journal
21703634A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.Wang KSJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs24647862.59E-05alcohol dependence21703634

eQTL of rs2464786 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 rs2464786 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 )
chr2130515443130516325E069-33810
chr2130514385130514525E070-35610
chr2130515443130516325E070-33810
chr2130551002130551500E070867
chr2130551711130551908E0701576
chr2130552014130552074E0701879
chr2130560809130560923E07010674
chr2130564612130564708E07014477
chr2130564745130564827E07014610
chr2130584827130584924E07034692
chr2130586417130586702E07036282
chr2130523139130523179E073-26956
chr2130523295130523397E073-26738
chr2130515443130516325E081-33810
chr2130538574130538722E081-11413
chr2130539541130539591E081-10544
chr2130539699130539767E081-10368
chr2130549450130549573E081-562
chr2130551002130551500E081867
chr2130551711130551908E0811576
chr2130552014130552074E0811879
chr2130577251130577386E08127116
chr2130578656130578729E08128521
chr2130579066130579412E08128931
chr2130579715130579843E08129580
chr2130579959130580074E08129824
chr2130515443130516325E082-33810
chr2130551002130551500E082867
chr2130551711130551908E0821576
chr2130552014130552074E0821879
chr2130564612130564708E08214477
chr2130564745130564827E08214610