ADHDgene Database

SNP Report

Basic Info

Name	rs10032613 dbSNP Ensembl
Location	Chr4:111021758(Fwd)
Variant Alleles	A/T
Ancestral Allele	T
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000514184) intron_variant(ENST00000394607; ENST00000302274; ENST00000514184; ENST00000506625; ENST00000506461; ENST00000503885) nc_transcript_variant(ENST00000506461)
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)
ELOVL6	ELOVL fatty acid elongase 6	4q25	1(0/0/1)

SNPs in LD with rs10032613 (count: 1) View in gBrowse (chr4:111021758..111026927 )

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]

rs10011926	NMD_transcript_variant; intron_variant; nc_transcript_variant	1(0/0/1)	1.0[ASW]; 0.936[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 0.872[LWK]; 1.0[MEX]; 0.855[MKK]; 0.968[TSI]; 0.895[YRI]