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	rs1940028 dbSNP Ensembl
Location	chr11:131842743(Fwd)
Variant Alleles	C/G
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000374784; ENST00000374786; ENST00000374791; ENST00000425719; ENST00000427481; ENST00000479431; ENST00000498764; ENST00000539799; ENST00000550167) nc_transcript_variant(ENST00000479431; ENST00000498764)
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
Yang L, 2013			P-value=0.0000474 P-value=0.0000474	The SNPs associated with P values of 1E-5 or lower The SNPs associated with P values of 1E-5 or lower	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs1940028 (count: 0) View in gBrowse (chr11:131842743..131842743 )