rs155155

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0106 (3092/29138,GnomAD)
G=0130 (3786/29118,TOPMED)
G=0121 (605/5008,1000G)
G=0036 (137/3854,ALSPAC)
G=0031 (116/3708,TWINSUK)
chr6:120169190 (GRCh38.p7) (6q22.31)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.120169190A>G
GRCh37.p13 chr 6NC_000006.11:g.120490336A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.745G=0.255
1000GenomesAmericanSub694A=0.940G=0.060
1000GenomesEast AsianSub1008A=0.899G=0.101
1000GenomesEuropeSub1006A=0.950G=0.050
1000GenomesGlobalStudy-wide5008A=0.879G=0.121
1000GenomesSouth AsianSub978A=0.930G=0.070
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.964G=0.036
The Genome Aggregation DatabaseAfricanSub8564A=0.770G=0.230
The Genome Aggregation DatabaseAmericanSub804A=0.930G=0.070
The Genome Aggregation DatabaseEast AsianSub1528A=0.912G=0.088
The Genome Aggregation DatabaseEuropeSub17942A=0.949G=0.051
The Genome Aggregation DatabaseGlobalStudy-wide29138A=0.893G=0.106
The Genome Aggregation DatabaseOtherSub300A=0.950G=0.050
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.870G=0.130
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.969G=0.031
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
rs1551550.0000832alcoholismpha002891
rs1551550.0000832alcohol dependence20201924

eQTL of rs155155 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 rs155155 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.