ADHDgene Database

SNP Report

Basic Info

Name	rs10267271 dbSNP Ensembl
Location	Chr7:73089419(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	downstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000324941; ENST00000451519)
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
VPS37D	vacuolar protein sorting 37 homolog D (S. cerevisiae)	7q11.23

SNPs in LD with rs10267271 (count: 2) View in gBrowse (chr7:73089419..73125263 )

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]

rs4363087	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant	1(1/0/0)	1.0[CEU]; 0.907[CHB]; 0.895[JPT]
rs941298	intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	0.831[CEU]; 0.81[TSI]