rs10903843

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0222 (6648/29868,GnomAD)
G=0246 (7165/29118,TOPMED)
G=0187 (936/5008,1000G)
G=0209 (806/3854,ALSPAC)
G=0209 (774/3708,TWINSUK)
chr10:2679970 (GRCh38.p7) (10p15.3)
AD
GWASdb2
1   publication(s)
See rs on genome
8 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.2679970A>G
GRCh37.p13 chr 10NC_000010.10:g.2722162A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.707G=0.293
1000GenomesAmericanSub694A=0.850G=0.150
1000GenomesEast AsianSub1008A=0.939G=0.061
1000GenomesEuropeSub1006A=0.786G=0.214
1000GenomesGlobalStudy-wide5008A=0.813G=0.187
1000GenomesSouth AsianSub978A=0.830G=0.170
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.791G=0.209
The Genome Aggregation DatabaseAfricanSub8694A=0.703G=0.297
The Genome Aggregation DatabaseAmericanSub836A=0.850G=0.150
The Genome Aggregation DatabaseEast AsianSub1622A=0.956G=0.044
The Genome Aggregation DatabaseEuropeSub18416A=0.795G=0.204
The Genome Aggregation DatabaseGlobalStudy-wide29868A=0.777G=0.222
The Genome Aggregation DatabaseOtherSub300A=0.660G=0.340
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.753G=0.246
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.791G=0.209
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
rs109038430.00061alcohol dependence24277619

eQTL of rs10903843 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 rs10903843 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 )
chr1027239102724020E0701748
chr1027241532724497E0701991
chr1027234852723635E0811323
chr1027236972723760E0811535
chr1027239102724020E0811748
chr1027457362745816E08123574
chr1027459342746041E08123772
chr1027460942746158E08123932