rs2087111

Homo sapiens
A>G / A>T
ZGRF1 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A==0411 (12300/29914,GnomAD)
A==0395 (11517/29118,TOPMED)
A==0277 (1387/5008,1000G)
A==0435 (1678/3854,ALSPAC)
A==0417 (1547/3708,TWINSUK)
chr4:112614924 (GRCh38.p7) (4q25)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.112614924A>G
GRCh38.p7 chr 4NC_000004.12:g.112614924A>T
GRCh37.p13 chr 4NC_000004.11:g.113536080A>G
GRCh37.p13 chr 4NC_000004.11:g.113536080A>T

Gene: ZGRF1, zinc finger GRF-type containing 1(minus strand)

Molecule type Change Amino acid[Codon] SO Term
ZGRF1 transcript variant 1NM_018392.4:c.N/AIntron Variant
ZGRF1 transcript variant X1XM_005263115.3:c.N/AIntron Variant
ZGRF1 transcript variant X2XM_011532091.2:c.N/AIntron Variant
ZGRF1 transcript variant X3XM_011532092.2:c.N/AIntron Variant
ZGRF1 transcript variant X5XM_011532093.2:c.N/AIntron Variant
ZGRF1 transcript variant X6XM_011532094.2:c.N/AIntron Variant
ZGRF1 transcript variant X11XM_011532096.2:c.N/AIntron Variant
ZGRF1 transcript variant X4XM_017008369.1:c.N/AIntron Variant
ZGRF1 transcript variant X5XM_017008370.1:c.N/AIntron Variant
ZGRF1 transcript variant X7XM_017008371.1:c.N/AIntron Variant
ZGRF1 transcript variant X15XM_017008372.1:c.N/AIntron Variant
ZGRF1 transcript variant X16XM_017008373.1:c.N/AIntron Variant
ZGRF1 transcript variant X12XM_011532097.2:c.N/AGenic Upstream Transcript Variant
ZGRF1 transcript variant X13XM_011532098.2:c.N/AGenic Upstream Transcript Variant
ZGRF1 transcript variant X14XM_011532099.2:c.N/AGenic Upstream Transcript Variant
ZGRF1 transcript variant X10XR_001741282.1:n.N/AIntron Variant
ZGRF1 transcript variant X8XR_938763.1:n.N/AIntron Variant
ZGRF1 transcript variant X9XR_938764.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.386G=0.614
1000GenomesAmericanSub694A=0.260G=0.740
1000GenomesEast AsianSub1008A=0.059G=0.941
1000GenomesEuropeSub1006A=0.437G=0.563
1000GenomesGlobalStudy-wide5008A=0.277G=0.723
1000GenomesSouth AsianSub978A=0.200G=0.800
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.435G=0.565
The Genome Aggregation DatabaseAfricanSub8718A=0.391G=0.609
The Genome Aggregation DatabaseAmericanSub836A=0.260G=0.740
The Genome Aggregation DatabaseEast AsianSub1616A=0.050G=0.950
The Genome Aggregation DatabaseEuropeSub18442A=0.458G=0.541
The Genome Aggregation DatabaseGlobalStudy-wide29914A=0.411G=0.588
The Genome Aggregation DatabaseOtherSub302A=0.470G=0.530
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.395G=0.604
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.417G=0.583
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
rs20871110.000836alcohol dependence20201924

eQTL of rs2087111 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr4:113536080LARP7ENSG00000174720.11A>G2.1704e-3-22066Cerebellar_Hemisphere

meQTL of rs2087111 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 )
chr45690508656905186E0704448
chr45692084956920899E07020211
chr45692104456921140E07020406
chr45692228756922376E07021649
chr45692344656923492E07022808
chr45692491156924971E07024273
chr45693410456934234E07033466
chr45693440756934486E07033769
chr45694911656949260E07048478
chr45690508656905186E0714448
chr45690508656905186E0744448
chr45691886156919356E08118223
chr45692084956920899E08120211
chr45692104456921140E08120406
chr45692117156921274E08120533
chr45692134356921789E08120705
chr45692189556922050E08121257
chr45692880756929256E08128169
chr45692940156929979E08128763
chr45693021356930297E08129575
chr45692084956920899E08220211
chr45692189556922050E08221257
chr45692228756922376E08221649
chr45692491156924971E08224273
chr45692880756929256E08228169
chr45692940156929979E08228763





Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr45691454056916546E06713902
chr45691454056916546E06813902
chr45691454056916546E06913902
chr45691454056916546E07013902
chr45691689356917009E07016255
chr45691701656917145E07016378
chr45691454056916546E07113902
chr45691454056916546E07213902
chr45691454056916546E07313902
chr45691454056916546E07413902
chr45691689356917009E07416255
chr45691701656917145E07416378
chr45691454056916546E08113902
chr45691689356917009E08116255
chr45691701656917145E08116378
chr45691454056916546E08213902
chr45691689356917009E08216255
chr45691701656917145E08216378