rs929892

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0346 (10368/29956,GnomAD)
A=0434 (12648/29118,TOPMED)
A=0485 (2427/5008,1000G)
A=0146 (564/3854,ALSPAC)
A=0128 (476/3708,TWINSUK)
chr16:82198839 (GRCh38.p7) (16q23.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 16NC_000016.10:g.82198839G>A
GRCh37.p13 chr 16NC_000016.9:g.82232444G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.176A=0.824
1000GenomesAmericanSub694G=0.530A=0.470
1000GenomesEast AsianSub1008G=0.621A=0.379
1000GenomesEuropeSub1006G=0.843A=0.157
1000GenomesGlobalStudy-wide5008G=0.515A=0.485
1000GenomesSouth AsianSub978G=0.520A=0.480
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.854A=0.146
The Genome Aggregation DatabaseAfricanSub8712G=0.268A=0.732
The Genome Aggregation DatabaseAmericanSub836G=0.480A=0.520
The Genome Aggregation DatabaseEast AsianSub1616G=0.674A=0.326
The Genome Aggregation DatabaseEuropeSub18490G=0.839A=0.160
The Genome Aggregation DatabaseGlobalStudy-wide29956G=0.653A=0.346
The Genome Aggregation DatabaseOtherSub302G=0.780A=0.220
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.565A=0.434
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.872A=0.128
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs9298921.82E-05alcohol consumption23743675

eQTL of rs929892 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 rs929892 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 )
chr168220238182202446E067-29998
chr168222352982224363E068-8081
chr168228172782281834E06849283
chr168228194582282010E06849501
chr168228202682282077E06849582
chr168228228182282335E06849837
chr168220238182202446E070-29998
chr168220238182202446E071-29998
chr168220467882204761E071-27683
chr168222352982224363E071-8081
chr168219396582194250E072-38194
chr168220238182202446E072-29998
chr168220238182202446E074-29998
chr168222281782223046E074-9398
chr168222352982224363E074-8081
chr168219499982195387E081-37057
chr168219568282195722E081-36722
chr168220238182202446E081-29998
chr168220467882204761E081-27683







Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr168220320982204552E067-27892
chr168220320982204552E068-27892
chr168220320982204552E069-27892
chr168220320982204552E070-27892
chr168220320982204552E071-27892
chr168220320982204552E072-27892
chr168220320982204552E073-27892
chr168220320982204552E074-27892
chr168220320982204552E081-27892
chr168220320982204552E082-27892