rs6687898

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0223 (6681/29924,GnomAD)
G=0243 (7097/29118,TOPMED)
G=0224 (1123/5008,1000G)
G=0262 (1011/3854,ALSPAC)
G=0268 (994/3708,TWINSUK)
chr1:110854694 (GRCh38.p7) (1p13.3)
AD
GWASdb2
1   publication(s)
See rs on genome
2 Enhancers around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.110854694A>G
GRCh37.p13 chr 1NC_000001.10:g.111397316A>G
OR11I1P pseudogeneNG_003221.2:g.696A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.828G=0.172
1000GenomesAmericanSub694A=0.710G=0.290
1000GenomesEast AsianSub1008A=0.883G=0.117
1000GenomesEuropeSub1006A=0.723G=0.277
1000GenomesGlobalStudy-wide5008A=0.776G=0.224
1000GenomesSouth AsianSub978A=0.700G=0.300
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.738G=0.262
The Genome Aggregation DatabaseAfricanSub8716A=0.817G=0.183
The Genome Aggregation DatabaseAmericanSub834A=0.690G=0.310
The Genome Aggregation DatabaseEast AsianSub1616A=0.879G=0.121
The Genome Aggregation DatabaseEuropeSub18456A=0.755G=0.244
The Genome Aggregation DatabaseGlobalStudy-wide29924A=0.776G=0.223
The Genome Aggregation DatabaseOtherSub302A=0.610G=0.390
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.756G=0.243
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.732G=0.268
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
rs66878980.00015alcohol dependence(early age of onset)20201924
rs66878980.00044alcohol dependence20201924

eQTL of rs6687898 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr1:111397316CD53ENSG00000143119.8A>G1.5723e-7-18459Frontal_Cortex_BA9
Chr1:111397316CD53ENSG00000143119.8A>G8.9309e-6-18459Cortex

meQTL of rs6687898 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 )
chr1111413648111414008E07416332
chr1111414054111414126E07416738

Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1111416015111416216E06718699
chr1111416227111416294E06718911
chr1111416347111416913E06719031
chr1111416015111416216E06818699
chr1111416227111416294E06818911
chr1111416347111416913E06819031
chr1111416919111417581E06819603
chr1111417654111418436E06820338
chr1111416347111416913E06919031
chr1111415395111415943E07118079
chr1111416015111416216E07118699
chr1111416227111416294E07118911
chr1111416347111416913E07119031
chr1111416919111417581E07119603
chr1111417654111418436E07120338
chr1111418524111418574E07121208
chr1111416347111416913E07219031
chr1111416919111417581E07219603
chr1111417654111418436E07220338
chr1111418524111418574E07221208
chr1111416015111416216E07418699
chr1111416227111416294E07418911
chr1111416347111416913E07419031
chr1111417654111418436E07420338
chr1111418524111418574E07421208