rs10042504

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0392 (11764/29944,GnomAD)
G=0422 (12308/29118,TOPMED)
G=0412 (2061/5008,1000G)
G=0363 (1398/3854,ALSPAC)
G=0362 (1343/3708,TWINSUK)
chr5:50386329 (GRCh38.p7) (5q11.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.50386329A>G
GRCh37.p13 chr 5NC_000005.9:g.49682163A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.491G=0.509
1000GenomesAmericanSub694A=0.670G=0.330
1000GenomesEast AsianSub1008A=0.527G=0.473
1000GenomesEuropeSub1006A=0.669G=0.331
1000GenomesGlobalStudy-wide5008A=0.588G=0.412
1000GenomesSouth AsianSub978A=0.640G=0.360
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.637G=0.363
The Genome Aggregation DatabaseAfricanSub8710A=0.478G=0.522
The Genome Aggregation DatabaseAmericanSub836A=0.660G=0.340
The Genome Aggregation DatabaseEast AsianSub1616A=0.485G=0.515
The Genome Aggregation DatabaseEuropeSub18480A=0.675G=0.324
The Genome Aggregation DatabaseGlobalStudy-wide29944A=0.607G=0.392
The Genome Aggregation DatabaseOtherSub302A=0.680G=0.320
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.577G=0.422
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.638G=0.362
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs100425040.0000915alcoholismpha002891
rs100425040.0000915alcohol dependence20201924

eQTL of rs10042504 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 rs10042504 in Fetal Brain

Probe ID Position Gene beta p-value
cg15950743chr5:49708521EMB-0.088830637498681.0654e-35

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.