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	rs11646411 dbSNP Ensembl
Location	Chr16:82746937(Fwd)
Variant Alleles	C/G
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000569144; ENST00000562601; ENST00000568770; ENST00000539548) intron_variant(ENST00000566620; ENST00000268613; ENST00000569144; ENST00000562601; ENST00000568770; ENST00000565636; ENST00000431540; ENST00000428848; ENST00000539548; ENST00000569455; ENST00000566333; ENST00000567445; ENST00000446376) nc_transcript_variant(ENST00000569455; ENST00000566333)
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
Lesch KP, 2008			ANOVA P-value=7.40E-06, Mean of ranks=79 ANOVA P-value=7.40E-06, Mean of ranks=79	one of the top 30 single SNPs located in gene regions (inclu...... one of the top 30 single SNPs located in gene regions (including 100kb of flanking sequences) ranked according to the mean rank calculated across three statistics; annotated by GWAS Catalog More...	Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs11646411 (count: 0) View in gBrowse (chr16:82746937..82746937 )