ADHDgene Database

SNP Report

Basic Info

Name	rs7638961 dbSNP Ensembl
Location	Chr3:113894394(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000295881; ENST00000467632; ENST00000460779; ENST00000383673)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
DRD3	dopamine receptor D3	3q13.3	8(1/7/0)

SNPs in LD with rs7638961 (count: 4) View in gBrowse (chr3:113881013..113894394 )

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]

rs226082	intron_variant	1(0/1/0)	0.926[ASW]; 0.8[CEU]; 0.918[CHD]; 0.833[JPT]; 0.91[MEX]; 0.929[TSI]
rs324029	intron_variant	1(0/1/0)	0.926[ASW]; 0.8[CEU]; 0.918[CHD]; 0.833[JPT]; 0.91[MEX]; 0.929[TSI]
rs7638876	intron_variant	1(1/0/0)	1.0[CEU]; 0.804[CHB]; 0.844[CHD]; 0.833[GIH]; 0.867[MEX]; 0.93[TSI]
rs6280	missense_variant	2(0/2/0)	1.0[ASW]; 1.0[CEU]; 0.905[CHB]; 0.972[CHD]; 1.0[GIH]; 0.833[JPT]; 0.923[LWK]; 0.954[MEX]; 1.0[MKK]; 1.0[TSI]; 1.0[YRI]