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	rs1805066 dbSNP Ensembl
Location	chr16:55719143(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	missense_variant. Polyphen Annotation: benign(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943) SIFT Annotation: tolerated(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
Consequence to Transcript	missense_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hahn MK, 2009	G:A			non-synonymous SNP in coding region of candidate gene SLC6A2 non-synonymous SNP in coding region of candidate gene SLC6A2	Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs1805066 (count: 0) View in gBrowse (chr16:55719143..55719143 )