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	rs2273505 dbSNP Ensembl
Location	Chr20:61990878(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000498043) intron_variant(ENST00000467563; ENST00000498043; ENST00000370263; ENST00000463705) nc_transcript_variant(ENST00000467563; ENST00000463705) upstream_gene_variant(ENST00000370257)
No. of Studies	2 (significant: 1; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Bobb AJ, 2005			allelic TDT P-value=0.71, OR=1.12 in case-control analysis; ...... allelic TDT P-value=0.71, OR=1.12 in case-control analysis; allelic TDT P-value=0.27, RR=1.63 in family-based analysis More...	non-significant association non-significant association	Non-significant
Lee J, 2008	G/A		P-value=0.085, X² (1df)=2.97 in all subtypes; P-v...... P-value=0.085, X² (1df)=2.97 in all subtypes; P-value=0.808, X² (1df)=0.059 in inattentive subtype; P-value=0.033, X² (1df)=4.568 in combined subtype; P-value=0.026 in FBAT analysis for hyperactive/impulsive symptoms More...	nominally significant evidence of association with the ADHD ...... nominally significant evidence of association with the ADHD combined subtype and with teacher-rated hyperactivity-impulsivity scores More...	Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs2273505 (count: 0) View in gBrowse (chr20:61990878..61990878 )