ADHDgene Database

SNP Report

Basic Info

Name	rs3196715 dbSNP Ensembl
Location	Chr3:179619860(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000467460; ENST00000464614; ENST00000485199; ENST00000263962; ENST00000468741; ENST00000465751; ENST00000476138; ENST00000472994; ENST00000487198; ENST00000463761; ENST00000469198; ENST00000474909) nc_transcript_variant(ENST00000487198; ENST00000462801; ENST00000474909) non_coding_exon_variant(ENST00000462801) upstream_gene_variant(ENST00000392649)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
PEX5L	peroxisomal biogenesis factor 5-like	3q27.1	1(0/0/1)

Approved Symbol	Approved Name	Location
PEX5L-AS2	PEX5L antisense RNA 2	3

SNPs in LD with rs3196715 (count: 1) View in gBrowse (chr3:179613236..179619860 )

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)	0.911[CEU]; 1.0[JPT]; 0.876[YRI]