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	rs174568 dbSNP Ensembl
Location	chr11:61593816(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; intron_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000517839) intron_variant(ENST00000257261; ENST00000421879; ENST00000448607; ENST00000522056) synonymous_variant(ENST00000522639; ENST00000574708) upstream_gene_variant(ENST00000278840; ENST00000517312; ENST00000518606; ENST00000521849)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
FADS2	fatty acid desaturase 2	11q12.2	3(3/0/0)
FADS1	fatty acid desaturase 1	11q12-q13.1	3(1/2/0)

Genes from other sources (count: 0)

SNPs in LD with rs174568 (count: 0) View in gBrowse (chr11:61593816..61593816 )