rs9881091

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0136 (4079/29872,GnomAD)
G=0174 (5068/29118,TOPMED)
G=0148 (742/5008,1000G)
G=0104 (399/3854,ALSPAC)
G=0107 (396/3708,TWINSUK)
chr3:164855523 (GRCh38.p7) (3q26.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.164855523T>G
GRCh37.p13 chr 3NC_000003.11:g.164573311T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.722G=0.278
1000GenomesAmericanSub694T=0.920G=0.080
1000GenomesEast AsianSub1008T=0.905G=0.095
1000GenomesEuropeSub1006T=0.907G=0.093
1000GenomesGlobalStudy-wide5008T=0.852G=0.148
1000GenomesSouth AsianSub978T=0.870G=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.896G=0.104
The Genome Aggregation DatabaseAfricanSub8706T=0.746G=0.254
The Genome Aggregation DatabaseAmericanSub836T=0.940G=0.060
The Genome Aggregation DatabaseEast AsianSub1614T=0.898G=0.102
The Genome Aggregation DatabaseEuropeSub18414T=0.911G=0.088
The Genome Aggregation DatabaseGlobalStudy-wide29872T=0.863G=0.136
The Genome Aggregation DatabaseOtherSub302T=0.910G=0.090
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.825G=0.174
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.893G=0.107
PMID Title Author Journal
24962325Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.Kapoor MDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs98810912.07E-08alcohol dependence (age at onset)24962325

eQTL of rs9881091 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 rs9881091 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.