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	rs1495099 dbSNP Ensembl
Location	Chr17:37784464(Fwd)
Variant Alleles	C/G
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000466381) intron_variant(ENST00000254079; ENST00000580825; ENST00000394271; ENST00000466381; ENST00000582680; ENST00000579000; ENST00000357165) upstream_gene_variant(ENST00000394267; ENST00000580772; ENST00000580029; ENST00000394265; ENST00000583446; ENST00000492037)
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
Laurin N, 2008(c)	G/C		P-value=0.586, X² (1 df)=0.297 in the categorical...... P-value=0.586, X² (1 df)=0.297 in the categorical analysis; P-value>0.05 in the quantitative analysis More...	no significant evidence of association no significant evidence of association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs1495099 (count: 0) View in gBrowse (chr17:37784464..37784464 )