Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 5 | NC_000005.10:g.54241168C>T |
GRCh37.p13 chr 5 | NC_000005.9:g.53536998C>T |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
ARL15 transcript | NM_019087.2:c. | N/A | Intron Variant |
ARL15 transcript variant X1 | XM_011543498.2:c. | N/A | Intron Variant |
ARL15 transcript variant X2 | XM_011543499.2:c. | N/A | Intron Variant |
ARL15 transcript variant X3 | XM_011543500.2:c. | N/A | Intron Variant |
ARL15 transcript variant X4 | XM_017009598.1:c. | N/A | Intron Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | C=0.425 | T=0.575 |
1000Genomes | American | Sub | 694 | C=0.530 | T=0.470 |
1000Genomes | East Asian | Sub | 1008 | C=0.573 | T=0.427 |
1000Genomes | Europe | Sub | 1006 | C=0.311 | T=0.689 |
1000Genomes | Global | Study-wide | 5008 | C=0.433 | T=0.567 |
1000Genomes | South Asian | Sub | 978 | C=0.350 | T=0.650 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | C=0.314 | T=0.686 |
The Genome Aggregation Database | African | Sub | 8698 | C=0.408 | T=0.592 |
The Genome Aggregation Database | American | Sub | 834 | C=0.510 | T=0.490 |
The Genome Aggregation Database | East Asian | Sub | 1610 | C=0.602 | T=0.398 |
The Genome Aggregation Database | Europe | Sub | 18442 | C=0.299 | T=0.700 |
The Genome Aggregation Database | Global | Study-wide | 29886 | C=0.353 | T=0.647 |
The Genome Aggregation Database | Other | Sub | 302 | C=0.240 | T=0.760 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | C=0.368 | T=0.631 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | C=0.310 | T=0.690 |
PMID | Title | Author | Journal |
---|---|---|---|
24962325 | Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. | Kapoor M | Drug Alcohol Depend |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs9292042 | 4.69E-07 | alcohol dependence (age at onset) | 24962325 |
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 ) |
---|---|---|---|---|
chr5 | 53524921 | 53525456 | E068 | -11542 |
chr5 | 53573941 | 53574185 | E069 | 36943 |
chr5 | 53574222 | 53574433 | E069 | 37224 |
chr5 | 53510666 | 53510874 | E070 | -26124 |
chr5 | 53511150 | 53511650 | E070 | -25348 |
chr5 | 53513271 | 53513323 | E070 | -23675 |
chr5 | 53573941 | 53574185 | E072 | 36943 |
chr5 | 53574222 | 53574433 | E072 | 37224 |
chr5 | 53574445 | 53574505 | E072 | 37447 |
chr5 | 53574222 | 53574433 | E074 | 37224 |
chr5 | 53574445 | 53574505 | E074 | 37447 |
chr5 | 53510666 | 53510874 | E081 | -26124 |
chr5 | 53511150 | 53511650 | E081 | -25348 |
chr5 | 53511150 | 53511650 | E082 | -25348 |
Chromosome | Start | End | Region | Distance(-/+:Up/Downstream) |
---|---|---|---|---|
chr5 | 53550606 | 53550896 | E071 | 13608 |