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	rs174697 dbSNP Ensembl
Location	chr22:19953832(Fwd)
Variant Alleles	A/G
Ancestral Allele	G
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000263207; ENST00000344269; ENST00000401994; ENST00000403184; ENST00000406259; ENST00000406522; ENST00000467943; ENST00000493893; ENST00000495096; ENST00000585066) intron_variant(ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000412786; ENST00000428707; ENST00000449653) NMD_transcript_variant(ENST00000207636)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Literature-origin genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
COMT	catechol-O-methyltransferase	22q11.21	29(7/22/0)
ARVCF	armadillo repeat gene deleted in velocardiofacial syndrome	22q11.21	1(1/0/0)

Genes from other sources (count: 1)

SNPs in LD with rs174697 (count: 0) View in gBrowse (chr22:19953832..19953832 )