ADHDgene Database

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Large-scale studies

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

SNP Report

Basic Info

Name	rs876493 dbSNP Ensembl
Location	chr17:37824545(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	5_prime_UTR_variant; downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000269582) downstream_gene_variant(ENST00000300658; ENST00000309862; ENST00000309889; ENST00000336308; ENST00000378011; ENST00000394250; ENST00000429199; ENST00000471896; ENST00000481171; ENST00000488876; ENST00000577337; ENST00000578283; ENST00000579146; ENST00000580611; ENST00000584850; ENST00000585269; LRG_210t1) intron_variant(ENST00000394246) upstream_gene_variant(ENST00000581428)
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
Hawi, Z., 2012	A:G	A	P-value=0.5879, X²=0.29, OR=1.08, 95% CI=0.82-1.4...... P-value=0.5879, X²=0.29, OR=1.08, 95% CI=0.82-1.40 More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 4)

Literature-origin genes (count: 1)

Genes from other sources (count: 3)

Approved Symbol	Approved Name	Location
TCAP	titin-cap	17q12
PGAP3	post-GPI attachment to proteins 3	17q21.2
STARD3	StAR-related lipid transfer (START) domain containing 3	17q11-q12

SNPs in LD with rs876493 (count: 0) View in gBrowse (chr17:37824545..37824545 )