rs7106300

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
C==0055 (1667/29982,GnomAD)
C==0068 (1997/29118,TOPMED)
C==0063 (315/5008,1000G)
C==0035 (135/3854,ALSPAC)
C==0042 (157/3708,TWINSUK)
chr11:5901477 (GRCh38.p7) (11p15.4)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 11NC_000011.10:g.5901477C>T
GRCh37.p13 chr 11NC_000011.9:g.5922707C>T
OR52E5 pseudogeneNG_005911.2:g.801C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.107T=0.893
1000GenomesAmericanSub694C=0.050T=0.950
1000GenomesEast AsianSub1008C=0.009T=0.991
1000GenomesEuropeSub1006C=0.051T=0.949
1000GenomesGlobalStudy-wide5008C=0.063T=0.937
1000GenomesSouth AsianSub978C=0.080T=0.920
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.035T=0.965
The Genome Aggregation DatabaseAfricanSub8728C=0.089T=0.911
The Genome Aggregation DatabaseAmericanSub838C=0.050T=0.950
The Genome Aggregation DatabaseEast AsianSub1612C=0.004T=0.996
The Genome Aggregation DatabaseEuropeSub18502C=0.043T=0.956
The Genome Aggregation DatabaseGlobalStudy-wide29982C=0.055T=0.944
The Genome Aggregation DatabaseOtherSub302C=0.090T=0.910
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.068T=0.931
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.042T=0.958
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
rs71063000.00037alcohol dependence20201924

eQTL of rs7106300 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 rs7106300 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.