rs17027360

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0131 (3933/29926,GnomAD)
G=0135 (3934/29116,TOPMED)
G=0135 (675/5008,1000G)
chr2:41259414 (GRCh38.p7) (2p22.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
1 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.41259414A>G
GRCh37.p13 chr 2NC_000002.11:g.41486554A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.811G=0.189
1000GenomesAmericanSub694A=0.910G=0.090
1000GenomesEast AsianSub1008A=0.793G=0.207
1000GenomesEuropeSub1006A=0.914G=0.086
1000GenomesGlobalStudy-wide5008A=0.865G=0.135
1000GenomesSouth AsianSub978A=0.930G=0.070
The Genome Aggregation DatabaseAfricanSub8708A=0.831G=0.169
The Genome Aggregation DatabaseAmericanSub836A=0.890G=0.110
The Genome Aggregation DatabaseEast AsianSub1598A=0.769G=0.231
The Genome Aggregation DatabaseEuropeSub18482A=0.893G=0.106
The Genome Aggregation DatabaseGlobalStudy-wide29926A=0.868G=0.131
The Genome Aggregation DatabaseOtherSub302A=0.900G=0.100
Trans-Omics for Precision MedicineGlobalStudy-wide29116A=0.864G=0.135
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
rs170273600.00033alcohol dependence20201924

eQTL of rs17027360 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 rs17027360 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.

Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr24149556641495617E0749012