rs6899567

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0141 (4248/29954,GnomAD)
A=0184 (5358/29118,TOPMED)
A=0129 (644/5008,1000G)
A=0064 (247/3854,ALSPAC)
A=0058 (215/3708,TWINSUK)
chr6:212595 (GRCh38.p7) (6p25.3)
AD
GWASdb2
2   publication(s)
See rs on genome
5 Enhancers around
7 Promoters around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.212595G>A
GRCh37.p13 chr 6NC_000006.11:g.212595G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.601A=0.399
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=0.941A=0.059
1000GenomesGlobalStudy-wide5008G=0.871A=0.129
1000GenomesSouth AsianSub978G=0.980A=0.020
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.936A=0.064
The Genome Aggregation DatabaseAfricanSub8706G=0.658A=0.342
The Genome Aggregation DatabaseAmericanSub838G=0.950A=0.050
The Genome Aggregation DatabaseEast AsianSub1622G=1.000A=0.000
The Genome Aggregation DatabaseEuropeSub18486G=0.934A=0.065
The Genome Aggregation DatabaseGlobalStudy-wide29954G=0.858A=0.141
The Genome Aggregation DatabaseOtherSub302G=0.940A=0.060
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.816A=0.184
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.942A=0.058
PMID Title Author Journal
19725835Binomial mixture model-based association tests under genetic heterogeneity.Zhou HAnn Hum Genet
22481050Genetic influences on craving for alcohol.Agrawal AAddict Behav

P-Value

SNP ID p-value Traits Study
rs68995673.76E-05alcohol craving with or without dependence22481050

eQTL of rs6899567 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 rs6899567 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 )
chr6188637189287E069-23308
chr6227391227566E06914796
chr6211994212056E070-539
chr6211994212056E072-539
chr6211994212056E073-539




Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr6235942236383E06723347
chr6235942236383E06823347
chr6235942236383E06923347
chr6235942236383E07123347
chr6235942236383E07223347
chr6235942236383E07323347
chr6235942236383E07423347