ADHDgene Database

SNP Report

Basic Info

Name	rs10405008 dbSNP Ensembl
Location	Chr19:57753643(Fwd)
Variant Alleles	C/G
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000354309; ENST00000414468; ENST00000535550)
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)
ZNF805	zinc finger protein 805	19q13.43	1(0/0/1)

SNPs in LD with rs10405008 (count: 2) View in gBrowse (chr19:57753643..57764770 )

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]

rs10421632	missense_variant	1(0/0/1)	0.886[CEU]; 0.927[CHB]; 0.961[CHD]; 0.955[GIH]; 0.863[JPT]; 1.0[MEX]; 0.977[TSI]
rs2014572	5_prime_UTR_variant; missense_variant	1(0/0/1)	0.886[CEU]; 0.927[CHB]; 0.805[JPT]