rs3005191

Homo sapiens
A>G
GPR158 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A==0493 (14737/29892,GnomAD)
A==0488 (14231/29118,TOPMED)
A==0414 (2071/5008,1000G)
A==0495 (1906/3854,ALSPAC)
G=0478 (1774/3708,TWINSUK)
chr10:25487247 (GRCh38.p7) (10p12.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.25487247A>G
GRCh37.p13 chr 10NC_000010.10:g.25776176A>G

Gene: GPR158, G protein-coupled receptor 158(plus strand)

Molecule type Change Amino acid[Codon] SO Term
GPR158 transcriptNM_020752.2:c.N/AIntron Variant
GPR158 transcript variant X2XM_017016452.1:c.N/AIntron Variant
GPR158 transcript variant X1XR_930512.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.480G=0.520
1000GenomesAmericanSub694A=0.500G=0.500
1000GenomesEast AsianSub1008A=0.178G=0.822
1000GenomesEuropeSub1006A=0.492G=0.508
1000GenomesGlobalStudy-wide5008A=0.414G=0.586
1000GenomesSouth AsianSub978A=0.420G=0.580
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.495G=0.505
The Genome Aggregation DatabaseAfricanSub8698A=0.506G=0.494
The Genome Aggregation DatabaseAmericanSub836A=0.500G=0.500
The Genome Aggregation DatabaseEast AsianSub1606A=0.225G=0.775
The Genome Aggregation DatabaseEuropeSub18452A=0.511G=0.488
The Genome Aggregation DatabaseGlobalStudy-wide29892A=0.493G=0.507
The Genome Aggregation DatabaseOtherSub300A=0.380G=0.620
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.488G=0.511
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.522G=0.478
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
rs30051910.000454alcohol dependence20201924

eQTL of rs3005191 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 rs3005191 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.