Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 12 | NC_000012.12:g.91932724T>C |
GRCh37.p13 chr 12 | NC_000012.11:g.92326500T>C |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
LOC105369901 transcript variant X2 | XR_001749253.1:n. | N/A | Intron Variant |
LOC105369901 transcript variant X3 | XR_001749254.1:n. | N/A | Intron Variant |
LOC105369901 transcript variant X4 | XR_001749255.1:n. | N/A | Intron Variant |
LOC105369901 transcript variant X5 | XR_001749256.1:n. | N/A | Intron Variant |
LOC105369901 transcript variant X1 | XR_945202.2:n. | N/A | Intron Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | T=0.641 | C=0.359 |
1000Genomes | American | Sub | 694 | T=0.440 | C=0.560 |
1000Genomes | East Asian | Sub | 1008 | T=0.096 | C=0.904 |
1000Genomes | Europe | Sub | 1006 | T=0.387 | C=0.613 |
1000Genomes | Global | Study-wide | 5008 | T=0.419 | C=0.581 |
1000Genomes | South Asian | Sub | 978 | T=0.470 | C=0.530 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | T=0.375 | C=0.625 |
The Genome Aggregation Database | African | Sub | 8700 | T=0.618 | C=0.382 |
The Genome Aggregation Database | American | Sub | 830 | T=0.420 | C=0.580 |
The Genome Aggregation Database | East Asian | Sub | 1594 | T=0.117 | C=0.883 |
The Genome Aggregation Database | Europe | Sub | 18406 | T=0.360 | C=0.639 |
The Genome Aggregation Database | Global | Study-wide | 29832 | T=0.424 | C=0.575 |
The Genome Aggregation Database | Other | Sub | 302 | T=0.350 | C=0.650 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | T=0.476 | C=0.523 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | T=0.364 | C=0.636 |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs11106345 | 0.00000722 | alcohol dependence | 23691058 |
rs11106345 | 0.00006 | alcohol dependence | 20201924 |
rs11106345 | 0.0000602 | alcoholism | pha002892 |
rs11106345 | 0.00037 | Alcohol dependence (early age of onset) | 20201924 |
Position (v37) | eGene | GeneID | Variant | p-value | TSS | Tissue | |
---|---|---|---|---|---|---|---|
There is no eQTL annotation for this SNP |
Probe ID | Position | Gene | beta | p-value | |||
---|---|---|---|---|---|---|---|
There is no meQTL annotation for this SNP |
There is no significant Hi-C chromatin interaction data for this SNP.
Chromosome | Start | End | Region | Distance ( -/+ : Up/Downstream ) |
---|---|---|---|---|
chr12 | 92285227 | 92285267 | E070 | -41233 |
chr12 | 92285612 | 92285704 | E070 | -40796 |
chr12 | 92285769 | 92286134 | E070 | -40366 |
chr12 | 92286204 | 92286429 | E070 | -40071 |
chr12 | 92286494 | 92286710 | E070 | -39790 |
chr12 | 92290484 | 92291024 | E070 | -35476 |
chr12 | 92291102 | 92291152 | E070 | -35348 |
chr12 | 92278137 | 92278506 | E081 | -47994 |
chr12 | 92285769 | 92286134 | E081 | -40366 |
chr12 | 92286204 | 92286429 | E081 | -40071 |
chr12 | 92286494 | 92286710 | E081 | -39790 |
chr12 | 92291102 | 92291152 | E081 | -35348 |
chr12 | 92285769 | 92286134 | E082 | -40366 |
chr12 | 92286204 | 92286429 | E082 | -40071 |