ADHDgene Database

SNP Report

Basic Info

Name	rs2001217 dbSNP Ensembl
Location	Chr15:91498246(Fwd)
Variant Alleles	A/C
Ancestral Allele	A
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000418476; ENST00000394275; ENST00000471780; ENST00000487875) intron_variant(ENST00000555155; ENST00000555737; ENST00000394258; ENST00000556774) nc_transcript_variant(ENST00000556774; ENST00000555737; ENST00000553321) non_coding_exon_variant(ENST00000553321) upstream_gene_variant(ENST00000554302; ENST00000557266; ENST00000556618; ENST00000556333; ENST00000557750)
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
RCCD1	RCC1 domain containing 1	15q26.1
UNC45A	unc-45 homolog A (C. elegans)	15q26.1

SNPs in LD with rs2001217 (count: 1) View in gBrowse (chr15:91450441..91498246 )

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]

rs2677744	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant	1(0/0/1)	0.836[CEU]