Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 13 | NC_000013.11:g.111328131A>G |
GRCh37.p13 chr 13 | NC_000013.10:g.111980478A>G |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
TEX29 transcript variant 1 | NM_001303133.1:c. | N/A | Intron Variant |
TEX29 transcript variant 2 | NM_152324.2:c. | N/A | Intron Variant |
TEX29 transcript variant X1 | XM_017020387.1:c. | N/A | Intron Variant |
TEX29 transcript variant X2 | XM_017020388.1:c. | N/A | Intron Variant |
TEX29 transcript variant X3 | XR_001749478.1:n. | N/A | Intron Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | A=0.232 | G=0.768 |
1000Genomes | American | Sub | 694 | A=0.100 | G=0.900 |
1000Genomes | East Asian | Sub | 1008 | A=0.142 | G=0.858 |
1000Genomes | Europe | Sub | 1006 | A=0.191 | G=0.809 |
1000Genomes | Global | Study-wide | 5008 | A=0.189 | G=0.811 |
1000Genomes | South Asian | Sub | 978 | A=0.240 | G=0.760 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | A=0.192 | G=0.808 |
The Genome Aggregation Database | African | Sub | 8708 | A=0.207 | G=0.793 |
The Genome Aggregation Database | American | Sub | 836 | A=0.090 | G=0.910 |
The Genome Aggregation Database | East Asian | Sub | 1618 | A=0.118 | G=0.882 |
The Genome Aggregation Database | Europe | Sub | 18488 | A=0.217 | G=0.782 |
The Genome Aggregation Database | Global | Study-wide | 29952 | A=0.204 | G=0.795 |
The Genome Aggregation Database | Other | Sub | 302 | A=0.150 | G=0.850 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | A=0.182 | G=0.817 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | A=0.198 | G=0.802 |
PMID | Title | Author | Journal |
---|---|---|---|
20201924 | Genome-wide association study of alcohol dependence implicates a region on chromosome 11. | Edenberg HJ | Alcohol Clin Exp Res |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs2479955 | 0.00047 | alcohol dependence | 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 ) |
---|---|---|---|---|
chr13 | 111931724 | 111931783 | E067 | -48695 |
chr13 | 111932959 | 111935073 | E067 | -45405 |
chr13 | 111936041 | 111936112 | E067 | -44366 |
chr13 | 111936460 | 111936664 | E067 | -43814 |
chr13 | 111939024 | 111939095 | E067 | -41383 |
chr13 | 111932959 | 111935073 | E068 | -45405 |
chr13 | 111950867 | 111950917 | E068 | -29561 |
chr13 | 111931003 | 111931161 | E069 | -49317 |
chr13 | 111931168 | 111931673 | E069 | -48805 |
chr13 | 111931724 | 111931783 | E069 | -48695 |
chr13 | 111932739 | 111932953 | E069 | -47525 |
chr13 | 111932959 | 111935073 | E069 | -45405 |
chr13 | 111936460 | 111936664 | E069 | -43814 |
chr13 | 111979363 | 111979413 | E070 | -1065 |
chr13 | 111980819 | 111980882 | E070 | 341 |
chr13 | 111981020 | 111981090 | E070 | 542 |
chr13 | 111987397 | 111987447 | E070 | 6919 |
chr13 | 111987473 | 111987557 | E070 | 6995 |
chr13 | 111987628 | 111988023 | E070 | 7150 |
chr13 | 111988119 | 111988169 | E070 | 7641 |
chr13 | 111988214 | 111988264 | E070 | 7736 |
chr13 | 112022696 | 112022736 | E070 | 42218 |
chr13 | 112022791 | 112022841 | E070 | 42313 |
chr13 | 112023217 | 112023279 | E070 | 42739 |
chr13 | 112023317 | 112023387 | E070 | 42839 |
chr13 | 112023598 | 112023839 | E070 | 43120 |
chr13 | 112024048 | 112024130 | E070 | 43570 |
chr13 | 111935403 | 111935606 | E071 | -44872 |
chr13 | 111936041 | 111936112 | E071 | -44366 |
chr13 | 111936460 | 111936664 | E071 | -43814 |
chr13 | 111936809 | 111936873 | E071 | -43605 |
chr13 | 111936910 | 111936960 | E071 | -43518 |
chr13 | 111937021 | 111937114 | E071 | -43364 |
chr13 | 111931724 | 111931783 | E072 | -48695 |
chr13 | 111931815 | 111932468 | E072 | -48010 |
chr13 | 111932545 | 111932620 | E072 | -47858 |
chr13 | 111932739 | 111932953 | E072 | -47525 |
chr13 | 111932959 | 111935073 | E072 | -45405 |
chr13 | 111936460 | 111936664 | E072 | -43814 |
chr13 | 111936809 | 111936873 | E072 | -43605 |
chr13 | 111936910 | 111936960 | E072 | -43518 |
chr13 | 111937021 | 111937114 | E072 | -43364 |
chr13 | 111945563 | 111945750 | E072 | -34728 |
chr13 | 111936041 | 111936112 | E073 | -44366 |
chr13 | 111938624 | 111938790 | E073 | -41688 |
chr13 | 111939024 | 111939095 | E073 | -41383 |
chr13 | 111939206 | 111939256 | E073 | -41222 |
chr13 | 111987628 | 111988023 | E074 | 7150 |
chr13 | 111980819 | 111980882 | E081 | 341 |
chr13 | 111987151 | 111987208 | E081 | 6673 |
chr13 | 111987397 | 111987447 | E081 | 6919 |
chr13 | 111987473 | 111987557 | E081 | 6995 |
chr13 | 111987628 | 111988023 | E081 | 7150 |
chr13 | 111988119 | 111988169 | E081 | 7641 |
chr13 | 111988214 | 111988264 | E081 | 7736 |
chr13 | 111996676 | 111997619 | E081 | 16198 |
chr13 | 112012232 | 112012384 | E081 | 31754 |
chr13 | 112012521 | 112012658 | E081 | 32043 |
chr13 | 111987628 | 111988023 | E082 | 7150 |
chr13 | 111988119 | 111988169 | E082 | 7641 |
chr13 | 111988214 | 111988264 | E082 | 7736 |