rs7867510

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0166 (4981/29948,GnomAD)
A=0154 (4510/29118,TOPMED)
A=0199 (995/5008,1000G)
A=0182 (703/3854,ALSPAC)
A=0177 (656/3708,TWINSUK)
chr9:15353412 (GRCh38.p7) (9p22.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.15353412G>A
GRCh37.p13 chr 9NC_000009.11:g.15353410G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.876A=0.124
1000GenomesAmericanSub694G=0.830A=0.170
1000GenomesEast AsianSub1008G=0.724A=0.276
1000GenomesEuropeSub1006G=0.796A=0.204
1000GenomesGlobalStudy-wide5008G=0.801A=0.199
1000GenomesSouth AsianSub978G=0.770A=0.230
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.818A=0.182
The Genome Aggregation DatabaseAfricanSub8718G=0.886A=0.114
The Genome Aggregation DatabaseAmericanSub836G=0.810A=0.190
The Genome Aggregation DatabaseEast AsianSub1618G=0.714A=0.286
The Genome Aggregation DatabaseEuropeSub18474G=0.821A=0.178
The Genome Aggregation DatabaseGlobalStudy-wide29948G=0.833A=0.166
The Genome Aggregation DatabaseOtherSub302G=0.790A=0.210
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.845A=0.154
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.823A=0.177
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
rs78675100.000366alcohol dependence21314694

eQTL of rs7867510 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 rs7867510 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 )
chr91535109015351434E069-1976
chr91535144415351554E069-1856
chr91535109015351434E071-1976
chr91535144415351554E071-1856
chr91535109015351434E072-1976
chr91537086715371337E07217457
chr91535109015351434E073-1976
chr91535144415351554E073-1856
chr91537060415370697E08117194
chr91537070715370851E08117297
chr91537086715371337E08117457
chr91536927415369476E08215864
chr91537060415370697E08217194
chr91537070715370851E08217297
chr91537086715371337E08217457






Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr91530558815308020E067-45390
chr91530558815308020E068-45390
chr91530558815308020E069-45390
chr91530558815308020E070-45390
chr91530558815308020E071-45390
chr91530558815308020E072-45390
chr91530558815308020E073-45390
chr91530558815308020E074-45390
chr91530558815308020E081-45390
chr91530558815308020E082-45390