rs10463741

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0164 (4932/29920,GnomAD)
G=0123 (3609/29118,TOPMED)
G=0187 (934/5008,1000G)
G=0195 (750/3854,ALSPAC)
G=0187 (694/3708,TWINSUK)
chr5:121444191 (GRCh38.p7) (5q23.1)
AD
GWASdb2
1   publication(s)
See rs on genome
2 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.121444191A>G
GRCh37.p13 chr 5NC_000005.9:g.120779886A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.980G=0.020
1000GenomesAmericanSub694A=0.840G=0.160
1000GenomesEast AsianSub1008A=0.501G=0.499
1000GenomesEuropeSub1006A=0.814G=0.186
1000GenomesGlobalStudy-wide5008A=0.813G=0.187
1000GenomesSouth AsianSub978A=0.890G=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.805G=0.195
The Genome Aggregation DatabaseAfricanSub8726A=0.964G=0.036
The Genome Aggregation DatabaseAmericanSub838A=0.860G=0.140
The Genome Aggregation DatabaseEast AsianSub1612A=0.524G=0.476
The Genome Aggregation DatabaseEuropeSub18442A=0.800G=0.199
The Genome Aggregation DatabaseGlobalStudy-wide29920A=0.835G=0.164
The Genome Aggregation DatabaseOtherSub302A=0.820G=0.180
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.876G=0.123
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.813G=0.187
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
rs104637410.0000847alcoholismpha002891
rs104637410.0000847alcohol dependence20201924

eQTL of rs10463741 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 rs10463741 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 )
chr5120750901120751274E070-28612
chr5120751497120751556E070-28330