rs1910370

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0397 (11898/29912,GnomAD)
A=0389 (11333/29116,TOPMED)
A=0317 (1587/5008,1000G)
A=0465 (1792/3854,ALSPAC)
A=0490 (1816/3708,TWINSUK)
chr2:67867965 (GRCh38.p7) (2p14)
AD
GWASdb2
1   publication(s)
See rs on genome
1 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.67867965G>A
GRCh37.p13 chr 2NC_000002.11:g.68095097G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.777A=0.223
1000GenomesAmericanSub694G=0.590A=0.410
1000GenomesEast AsianSub1008G=0.776A=0.224
1000GenomesEuropeSub1006G=0.509A=0.491
1000GenomesGlobalStudy-wide5008G=0.683A=0.317
1000GenomesSouth AsianSub978G=0.710A=0.290
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.535A=0.465
The Genome Aggregation DatabaseAfricanSub8714G=0.744A=0.256
The Genome Aggregation DatabaseAmericanSub838G=0.570A=0.430
The Genome Aggregation DatabaseEast AsianSub1610G=0.786A=0.214
The Genome Aggregation DatabaseEuropeSub18450G=0.521A=0.478
The Genome Aggregation DatabaseGlobalStudy-wide29912G=0.602A=0.397
The Genome Aggregation DatabaseOtherSub300G=0.570A=0.430
Trans-Omics for Precision MedicineGlobalStudy-wide29116G=0.610A=0.389
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.510A=0.490
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
rs19103700.000778alcohol consumption (maxi-drinks)24277619

eQTL of rs1910370 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 rs1910370 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 )
chr26807315168073975E067-21122
chr26807576568075965E067-19132
chr26807614368076196E067-18901
chr26807576568075965E068-19132
chr26807614368076196E068-18901
chr26807671168076770E068-18327
chr26810696668108129E06811869
chr26807576568075965E069-19132
chr26807614368076196E069-18901
chr26805145168051652E070-43445
chr26805226168052332E070-42765
chr26805265668052948E070-42149
chr26805297868053065E070-42032
chr26805330768053352E070-41745
chr26807279268073087E070-22010
chr26807315168073975E070-21122
chr26807614368076196E070-18901
chr26810452268104780E0709425
chr26810507568105153E0709978
chr26810685768106925E07011760
chr26810696668108129E07011869
chr26807576568075965E071-19132
chr26807614368076196E071-18901
chr26807576568075965E072-19132
chr26807614368076196E072-18901
chr26807576568075965E073-19132
chr26807614368076196E073-18901
chr26807315168073975E074-21122
chr26807576568075965E074-19132
chr26807614368076196E074-18901
chr26805145168051652E081-43445
chr26805297868053065E081-42032
chr26807917268079694E081-15403
chr26807971068079801E081-15296
chr26809524868095401E081151
chr26809544268095700E081345
chr26810452268104780E0819425
chr26810452268104780E0829425
chr26810507568105153E0829978










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr26813360968133686E08138512