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Hot SNP List
Total result: 23
rs_ID | Location | Functional Annotation | No. of Studies (significant/non-significant/trend) | Related Genes |
---|---|---|---|---|
rs27072 | Chr5:1394522(Fwd) | 3_prime_UTR_variant | 7 (3/4/0) | SLC6A3 |
rs1051312 | Chr20:10287088(Fwd) | 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 10 (1/9/0) | SNAP25 SNAP25-AS1 |
rs3746544 | Chr20:10287084(Fwd) | 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 13 (5/8/0) | SNAP25 SNAP25-AS1 |
rs6265 | Chr11:27679916(Fwd) | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant | 12 (3/9/0) | BDNF BDNF-AS1 |
rs2519152 | Chr9:136509634(Fwd) | downstream_gene_variant; intron_variant | 6 (2/4/0) | DBH |
rs362987 | Chr20:10277452(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 5 (1/4/0) | SNAP25 SNAP25-AS1 |
rs998424 | Chr16:55731946(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 7 (2/5/0) | NET1 SLC6A2 |
rs3785157 | Chr16:55729836(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 5 (3/2/0) | NET1 SLC6A2 |
rs6347 | Chr5:1411412(Fwd) | downstream_gene_variant; synonymous_variant | 6 (0/6/0) | SLC6A3 |
rs5569 | Chr16:55731835(Fwd) | downstream_gene_variant; synonymous_variant; upstream_gene_variant | 6 (1/4/1) | NET1 SLC6A2 |
rs11568324 | Chr16:55726058(Fwd) | intron_variant | 5 (4/1/0) | NET1 SLC6A2 |
rs3785143 | Chr16:55695106(Fwd) | intron_variant | 6 (5/1/0) | NET1 SLC6A2 |
rs40184 | Chr5:1395077(Fwd) | intron_variant | 7 (2/5/0) | SLC6A3 |
rs2242447 | Chr16:55735912(Fwd) | intron_variant | 6 (1/5/0) | NET1 SLC6A2 |
rs363006 | Chr20:10280083(Fwd) | intron_variant; nc_transcript_variant | 6 (0/6/0) | SNAP25 SNAP25-AS1 |
rs1108580 | Chr9:136505114(Fwd) | intron_variant; splice_region_variant; synonymous_variant | 5 (1/4/0) | DBH |
rs4680 | Chr22:19951271(Fwd) | NMD_transcript_variant; downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 22 (4/18/0) | COMT MIR4761 |
rs1843809 | Chr12:72348698(Fwd) | NMD_transcript_variant; intron_variant | 5 (3/2/0) | TPH2 |
rs6296 | Chr6:78172260(Fwd) | synonymous_variant | 10 (3/7/0) | HTR1B |
rs2652511 | Chr5:1446389(Fwd) | upstream_gene_variant | 5 (3/1/1) | SLC6A3 |
rs1611115 | Chr9:136500515(Fwd) | upstream_gene_variant | 6 (1/5/0) | DBH |
rs11564750 | Chr5:1447762(Fwd) | upstream_gene_variant | 6 (3/3/0) | SLC6A3 |
rs1800544 | Chr10:112836503(Fwd) | upstream_gene_variant | 11 (1/10/0) | ADRA2A |