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

SNP Report

Basic Info
Name rs1495099 dbSNP Ensembl
Location chr17:37784464(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000254079; ENST00000579000; ENST00000580825; ENST00000582680)
upstream_gene_variant(ENST00000394265; ENST00000394267; ENST00000492037; ENST00000580029; ENST00000580772; ENST00000583446)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Laurin N, 2008(c) G/C P-value=0.586, X2 (1 df)=0.297 in the categorical...... P-value=0.586, X2 (1 df)=0.297 in the categorical analysis; P-value>0.05 in the quantitative analysis More... no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs1495099 (count: 0) View in gBrowse (chr17:37784464..37784464 )