rs9549880

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0236 (7060/29906,GnomAD)
A=0230 (6709/29118,TOPMED)
A=0261 (1306/5008,1000G)
A=0279 (1076/3854,ALSPAC)
A=0272 (1010/3708,TWINSUK)
chr13:112207874 (GRCh38.p7) (13q34)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.112207874G>A
GRCh38.p7 chr 13NC_000013.11:g.112207874G>T
GRCh38.p7 chr 13 alt locus HSCHR13_1_CTG1NT_187592.1:g.25000G>A
GRCh38.p7 chr 13 alt locus HSCHR13_1_CTG1NT_187592.1:g.25000G>T
GRCh37.p13 chr 13NC_000013.10:g.112862188G>A
GRCh37.p13 chr 13NC_000013.10:g.112862188G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.840A=0.160
1000GenomesAmericanSub694G=0.850A=0.150
1000GenomesEast AsianSub1008G=0.700A=0.300
1000GenomesEuropeSub1006G=0.713A=0.287
1000GenomesGlobalStudy-wide5008G=0.739A=0.261
1000GenomesSouth AsianSub978G=0.590A=0.410
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.721A=0.279
The Genome Aggregation DatabaseAfricanSub8710G=0.833T=0.000
The Genome Aggregation DatabaseAmericanSub838G=0.880T=0.00,
The Genome Aggregation DatabaseEast AsianSub1606G=0.711T=0.000
The Genome Aggregation DatabaseEuropeSub18452G=0.730T=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29906G=0.763T=0.000
The Genome Aggregation DatabaseOtherSub300G=0.770T=0.00,
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.769A=0.230
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.728A=0.272
PMID Title Author Journal
24277619ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample.Quillen EEAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs95498800.000593alcohol consumption (maxi-drinks)24277619

eQTL of rs9549880 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 rs9549880 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.