Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 4 | NC_000004.12:g.99133676C>T |
GRCh37.p13 chr 4 | NC_000004.11:g.100054827C>T |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
ADH4 transcript variant 3 | NM_000670.4:c. | N/A | Intron Variant |
ADH4 transcript variant 1 | NM_001306171.1:c. | N/A | Intron Variant |
ADH4 transcript variant 2 | NM_001306172.1:c. | N/A | Intron Variant |
ADH4 transcript variant X1 | XM_017007713.1:c. | N/A | Intron Variant |
ADH4 transcript variant X2 | XM_017007714.1:c. | N/A | Intron Variant |
ADH4 transcript variant X3 | XM_017007715.1:c. | N/A | Intron Variant |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
LOC100507053 transcript | NR_037884.1:n.550C>T | C>T | Non Coding Transcript Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | C=0.139 | T=0.861 |
1000Genomes | American | Sub | 694 | C=0.230 | T=0.770 |
1000Genomes | East Asian | Sub | 1008 | C=0.001 | T=0.999 |
1000Genomes | Europe | Sub | 1006 | C=0.303 | T=0.697 |
1000Genomes | Global | Study-wide | 5008 | C=0.153 | T=0.847 |
1000Genomes | South Asian | Sub | 978 | C=0.120 | T=0.880 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | C=0.308 | T=0.692 |
The Genome Aggregation Database | African | Sub | 8718 | C=0.175 | T=0.825 |
The Genome Aggregation Database | American | Sub | 838 | C=0.250 | T=0.750 |
The Genome Aggregation Database | East Asian | Sub | 1620 | C=0.002 | T=0.998 |
The Genome Aggregation Database | Europe | Sub | 18444 | C=0.315 | T=0.684 |
The Genome Aggregation Database | Global | Study-wide | 29920 | C=0.255 | T=0.744 |
The Genome Aggregation Database | Other | Sub | 300 | C=0.310 | T=0.690 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | C=0.243 | T=0.756 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | C=0.316 | T=0.684 |
PMID | Title | Author | Journal |
---|---|---|---|
24166409 | Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. | Gelernter J | Mol Psychiatry |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs6532798 | 7E-06 | alcohol dependence | 24166409 |
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 ) |
---|---|---|---|---|
chr4 | 100006643 | 100006704 | E070 | -48123 |
chr4 | 100006873 | 100006947 | E070 | -47880 |
chr4 | 100012091 | 100012363 | E071 | -42464 |
chr4 | 100006873 | 100006947 | E081 | -47880 |
chr4 | 100007948 | 100008019 | E081 | -46808 |
chr4 | 100006643 | 100006704 | E082 | -48123 |
chr4 | 100006873 | 100006947 | E082 | -47880 |
Chromosome | Start | End | Region | Distance(-/+:Up/Downstream) |
---|---|---|---|---|
chr4 | 100008829 | 100008950 | E067 | -45877 |
chr4 | 100009042 | 100010625 | E067 | -44202 |
chr4 | 100010636 | 100011572 | E067 | -43255 |
chr4 | 100008829 | 100008950 | E068 | -45877 |
chr4 | 100009042 | 100010625 | E068 | -44202 |
chr4 | 100010636 | 100011572 | E068 | -43255 |
chr4 | 100008645 | 100008721 | E069 | -46106 |
chr4 | 100008829 | 100008950 | E069 | -45877 |
chr4 | 100009042 | 100010625 | E069 | -44202 |
chr4 | 100010636 | 100011572 | E069 | -43255 |
chr4 | 100008158 | 100008256 | E070 | -46571 |
chr4 | 100008370 | 100008613 | E070 | -46214 |
chr4 | 100008645 | 100008721 | E070 | -46106 |
chr4 | 100008829 | 100008950 | E070 | -45877 |
chr4 | 100009042 | 100010625 | E070 | -44202 |
chr4 | 100010636 | 100011572 | E070 | -43255 |
chr4 | 100009042 | 100010625 | E071 | -44202 |
chr4 | 100010636 | 100011572 | E071 | -43255 |
chr4 | 100008829 | 100008950 | E072 | -45877 |
chr4 | 100009042 | 100010625 | E072 | -44202 |
chr4 | 100010636 | 100011572 | E072 | -43255 |
chr4 | 100008829 | 100008950 | E073 | -45877 |
chr4 | 100009042 | 100010625 | E073 | -44202 |
chr4 | 100010636 | 100011572 | E073 | -43255 |
chr4 | 100009042 | 100010625 | E074 | -44202 |
chr4 | 100010636 | 100011572 | E074 | -43255 |
chr4 | 100008645 | 100008721 | E081 | -46106 |
chr4 | 100008829 | 100008950 | E081 | -45877 |
chr4 | 100009042 | 100010625 | E081 | -44202 |
chr4 | 100010636 | 100011572 | E081 | -43255 |
chr4 | 100007472 | 100007769 | E082 | -47058 |
chr4 | 100008158 | 100008256 | E082 | -46571 |
chr4 | 100008370 | 100008613 | E082 | -46214 |
chr4 | 100008645 | 100008721 | E082 | -46106 |
chr4 | 100008829 | 100008950 | E082 | -45877 |
chr4 | 100009042 | 100010625 | E082 | -44202 |
chr4 | 100010636 | 100011572 | E082 | -43255 |