ADHDgene Database

SNP Report

Basic Info

Name	rs10900072 dbSNP Ensembl
Location	Chr10:45066922(Fwd)
Variant Alleles	T/G
Ancestral Allele	G
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs10900072 (count: 8) View in gBrowse (chr10:45066922..45104415 )

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

rs_ID	Functional Annotation	#studies(significant/non-significant/trend)	r²[population]

rs7069381		1(0/1/0)	1.0[CEU]; 0.843[GIH]; 0.872[MEX]; 0.872[TSI]
rs11239157		1(0/1/0)	1.0[CEU]; 1.0[CHB]; 0.976[CHD]; 0.913[GIH]; 1.0[JPT]; 0.873[MEX]; 0.872[TSI]
rs10900075		1(0/1/0)	1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 0.913[GIH]; 0.898[JPT]; 0.873[MEX]; 0.872[TSI]
rs7083920		1(0/1/0)	1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 0.913[GIH]; 1.0[JPT]; 0.872[MEX]; 0.872[TSI]
rs1021055		1(0/1/0)	1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 0.913[GIH]; 1.0[JPT]; 0.873[MEX]; 0.872[TSI]
rs1999774		1(0/1/0)	1.0[CEU]; 1.0[CHB]; 0.976[CHD]; 0.912[GIH]; 1.0[JPT]; 0.873[MEX]; 0.872[TSI]
rs2061971	intron_variant; nc_transcript_variant	1(0/1/0)	1.0[CEU]; 0.806[CHD]; 0.843[GIH]; 0.829[MEX]; 0.848[TSI]
rs899889		1(0/1/0)	0.96[CEU]; 1.0[CHB]; 1.0[CHD]; 0.913[GIH]; 1.0[JPT]; 0.873[MEX]; 0.872[TSI]