rs6505955

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0205 (5508/26820,GnomAD)
G=0239 (1198/5008,1000G)
G=0137 (527/3854,ALSPAC)
G=0131 (487/3708,TWINSUK)
chr18:1731153 (GRCh38.p7) (18p11.32)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.1731153A>G
GRCh37.p13 chr 18NC_000018.9:g.1731154A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.699G=0.301
1000GenomesAmericanSub694A=0.740G=0.260
1000GenomesEast AsianSub1008A=0.715G=0.285
1000GenomesEuropeSub1006A=0.861G=0.139
1000GenomesGlobalStudy-wide5008A=0.761G=0.239
1000GenomesSouth AsianSub978A=0.800G=0.200
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.863G=0.137
The Genome Aggregation DatabaseAfricanSub7988A=0.686G=0.314
The Genome Aggregation DatabaseAmericanSub758A=0.700G=0.300
The Genome Aggregation DatabaseEast AsianSub1514A=0.711G=0.289
The Genome Aggregation DatabaseEuropeSub16278A=0.858G=0.141
The Genome Aggregation DatabaseGlobalStudy-wide26820A=0.794G=0.205
The Genome Aggregation DatabaseOtherSub282A=0.880G=0.120
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.869G=0.131
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
rs65059550.000961alcohol dependence20201924

eQTL of rs6505955 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 rs6505955 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.