ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Hot SNP List

Search by: Type = SNP, No. of All Studies >= 5

Total result: 26

rs_ID Location Functional Annotation No. of Studies (significant/non-significant/trend) Related Genes
rs3785157 chr16:55729836(Fwd) downstream_gene_variant; intron_variant; upstream_gene_variant 5 (3/2/0) SLC6A2
rs11568324 chr16:55726058(Fwd) intron_variant 5 (4/1/0) SLC6A2
rs362987 chr20:10277452(Fwd) downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant 5 (1/4/0) SNAP25 SNAP25-AS1
rs1386493 chr12:72355179(Fwd) intron_variant; nc_transcript_variant 5 (2/3/0) TPH2
rs8636 chr20:10287742(Fwd) 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant 5 (2/3/0) SNAP25 SNAP25-AS1
rs6311 chr13:47471478(Fwd) upstream_gene_variant 5 (1/4/0) HTR2A
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 6 (1/5/0) DBH
rs2652511 chr5:1446389(Fwd) upstream_gene_variant 6 (4/1/1) SLC6A3
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) SLC6A2
rs11564750 chr5:1447762(Fwd) upstream_gene_variant 6 (3/3/0) SLC6A3
rs1843809 chr12:72348698(Fwd) intron_variant; nc_transcript_variant 6 (4/2/0) TPH2
rs3785143 chr16:55695106(Fwd) intron_variant 6 (5/1/0) SLC6A2
rs998424 chr16:55731946(Fwd) downstream_gene_variant; intron_variant; upstream_gene_variant 7 (2/5/0) SLC6A2
rs2519152 chr9:136509634(Fwd) downstream_gene_variant; intron_variant 7 (2/5/0) DBH
rs40184 chr5:1395077(Fwd) intron_variant 7 (2/5/0) SLC6A3
rs1611115 chr9:136500515(Fwd) upstream_gene_variant 7 (2/5/0) DBH
rs2242447 chr16:55735912(Fwd) intron_variant 7 (2/5/0) SLC6A2 NET1
rs27072 chr5:1394522(Fwd) 3_prime_UTR_variant 7 (3/4/0) SLC6A3
rs6296 chr6:78172260(Fwd) synonymous_variant 10 (3/7/0) HTR1B
rs1800544 chr10:112836503(Fwd) upstream_gene_variant 12 (1/11/0) ADRA2A
rs1051312 chr20:10287088(Fwd) 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant 12 (2/10/0) SNAP25 SNAP25-AS1
rs6265 chr11:27679916(Fwd) 3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant 13 (3/10/0) BDNF BDNF-AS
rs3746544 chr20:10287084(Fwd) 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant 16 (7/9/0) SNAP25 SNAP25-AS1
rs4680 chr22:19951271(Fwd) downstream_gene_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant 23 (4/19/0) COMT MIR4761