ADHDgene Database

SNP Report

Basic Info

Name	rs2302741 dbSNP Ensembl
Location	Chr3:179605294(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000467460; ENST00000464614; ENST00000476138; ENST00000468741; ENST00000485199; ENST00000465751; ENST00000263962; ENST00000472994; ENST00000467440; ENST00000491640; ENST00000496721; ENST00000469198; ENST00000463761; ENST00000487198; ENST00000392649) nc_transcript_variant(ENST00000487198)
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)
PEX5L	peroxisomal biogenesis factor 5-like	3q27.1	1(0/0/1)

SNPs in LD with rs2302741 (count: 1) View in gBrowse (chr3:179605294..179613236 )

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]

rs9842394	intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/0/1)	1.0[CHB]