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

Detail ...

SNP Report

Basic Info

Name	rs979605 dbSNP Ensembl
Location	chrX:43601363(Fwd)
Variant Alleles	A/G
Ancestral Allele	A
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000338702; ENST00000542639) upstream_gene_variant(ENST00000490604)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi, Z., 2012	G:A	A	P-value=0.632, X²=0.229, OR=1.12, 95% CI=0.70-1.7...... P-value=0.632, X²=0.229, OR=1.12, 95% CI=0.70-1.78 More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant
Domschke K, 2005	A/G		allelic TDT P-value=0.71, X²=0.2, df=1 allelic TDT P-value=0.71, X²=0.2, df=1	did not show any significant distortion in the transmission ...... did not show any significant distortion in the transmission to ADHD cases More...	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
MAOA	monoamine oxidase A	Xp11.4-p11.3	20(13/7/0)

Genes from other sources (count: 0)

SNPs in LD with rs979605 (count: 61) View in gBrowse (chrX:43420059..43612708 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 61)

rs_ID	Functional Annotation	r²[population]
rs909525	intron_variant; nc_transcript_variant	0.858[CHB]; 0.843[CHD]; 0.814[JPT]
rs3859959		0.81[CEU]
rs5906729	intron_variant; nc_transcript_variant	0.877[CEU]; 0.858[CHB]; 0.814[JPT]
rs5906883	intron_variant; nc_transcript_variant	0.877[CEU]; 0.843[CHD]; 0.814[JPT]; 0.872[GIH]
rs5906974	intron_variant; nc_transcript_variant	0.935[CEU]; 0.858[CHB]; 0.814[JPT]
rs5951049		0.823[CEU]
rs4824392		0.823[CEU]
rs2283725	intron_variant; nc_transcript_variant	0.858[CHB]; 0.904[CHD]; 0.814[JPT]
rs5951044		0.823[CEU]
rs4986545		0.823[CEU]
rs3027397	intron_variant; nc_transcript_variant	0.858[CHB]; 0.814[JPT]
rs4239988		0.822[CEU]
rs1339778		0.809[CEU]
rs6609257		0.839[CHD]
rs4083948		0.823[CEU]
rs979606	intron_variant; upstream_gene_variant	1.0[CEU]; 1.0[TSI]; 1.0[CHB]; 1.0[CHD]; 1.0[JPT]; 1.0[GIH]; 0.936[MEX]
rs2072743	intron_variant; upstream_gene_variant	0.931[TSI]; 1.0[CHB]; 1.0[CHD]; 0.873[JPT]; 0.88[MEX]
rs3027410	downstream_gene_variant	0.93[CEU]; 0.964[TSI]; 0.931[CHB]; 1.0[CHD]; 1.0[JPT]; 0.906[GIH]; 0.824[LWK]; 0.835[MKK]
rs6520894	intron_variant; nc_transcript_variant	0.877[CEU]; 0.858[CHB]; 0.843[CHD]; 0.814[JPT]; 0.872[GIH]
rs5951043		0.823[CEU]
rs4986550		0.823[CEU]
rs2000019		0.823[CEU]
rs6610814		0.823[CEU]
rs3859958		0.877[CEU]
rs12558025		0.877[CEU]
rs3810709	intron_variant; nc_transcript_variant	0.931[TSI]; 1.0[CHB]; 0.967[CHD]; 0.87[JPT]; 0.877[MEX]
rs28401570	intron_variant; nc_transcript_variant	1.0[CEU]; 1.0[TSI]; 1.0[CHB]; 0.967[CHD]; 0.873[JPT]; 1.0[GIH]; 0.936[MEX]
rs4986546		0.823[CEU]
rs5906261		0.877[CEU]
rs1339777		0.823[CEU]
rs5906957	intron_variant; nc_transcript_variant	0.858[CHB]; 0.814[JPT]
rs2310820		0.877[CEU]
rs1465108	intron_variant; nc_transcript_variant	0.876[CEU]; 0.858[CHB]; 0.838[CHD]; 0.814[JPT]; 0.872[GIH]
rs1538642		0.823[CEU]
rs4986548		0.823[CEU]
rs5906154		0.877[CEU]
rs5905613		0.877[CEU]
rs5951048		0.817[CEU]
rs5951055		0.823[CEU]
rs5906898		0.823[CEU]
rs4986516		0.866[CEU]
rs6610823		0.823[CEU]
rs3027396	intron_variant; nc_transcript_variant	0.858[CHB]; 0.903[CHD]; 0.811[JPT]
rs5906938	intron_variant; nc_transcript_variant	0.877[CEU]; 0.858[CHB]; 0.843[CHD]; 0.814[JPT]; 0.872[GIH]
rs3027398	intron_variant; nc_transcript_variant	0.858[CHB]; 0.904[CHD]; 0.814[JPT]
rs5951054		0.823[CEU]
rs1339779		0.823[CEU]
rs28556796	intron_variant; nc_transcript_variant	1.0[CEU]; 1.0[TSI]; 1.0[CHB]; 0.967[CHD]; 0.873[JPT]; 1.0[GIH]; 0.936[MEX]
rs1339776		0.823[CEU]
rs4301558	upstream_gene_variant	0.877[CEU]; 0.858[CHB]
rs1800659	intron_variant; nc_transcript_variant	0.935[CEU]; 0.932[TSI]; 1.0[CHB]; 0.935[CHD]; 0.873[JPT]; 0.936[GIH]; 0.88[MEX]
rs6610846	intron_variant; nc_transcript_variant	0.931[TSI]; 1.0[CHB]; 0.967[CHD]; 0.873[JPT]; 0.88[MEX]
rs6610813		0.823[CEU]
rs2064070	downstream_gene_variant	0.935[CEU]; 0.964[TSI]; 0.931[CHB]; 1.0[CHD]; 1.0[JPT]; 0.907[GIH]; 0.828[LWK]; 0.834[MKK]
rs5991694		0.823[CEU]
rs929094		0.823[CEU]
rs4986551		0.823[CEU]
rs5906893	intron_variant; nc_transcript_variant	0.877[CEU]; 0.857[CHB]; 0.843[CHD]; 0.814[JPT]; 0.872[GIH]
rs3027401	downstream_gene_variant; intron_variant	1.0[CEU]; 1.0[TSI]; 1.0[CHB]; 1.0[CHD]; 0.873[JPT]; 1.0[GIH]; 0.936[MEX]
rs1465107	intron_variant; nc_transcript_variant	0.858[CHB]; 0.812[JPT]
rs5953385	intron_variant; nc_transcript_variant	0.877[CEU]; 0.858[CHB]; 0.843[CHD]; 0.814[JPT]; 0.872[GIH]