ADHDgene Database

SNP Report

Basic Info

Name	rs7660952 dbSNP Ensembl
Location	Chr4:91830371(Fwd)
Variant Alleles	T/A
Ancestral Allele	A
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000505073; ENST00000513522; ENST00000509109) intron_variant(ENST00000509176; ENST00000505073; ENST00000513522; ENST00000503421; ENST00000333691; ENST00000509109; ENST00000515693) nc_transcript_variant(ENST00000515693)
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)
FAM190A	family with sequence similarity 190, member A	4q22.1	1(1/0/0)

SNPs in LD with rs7660952 (count: 1) View in gBrowse (chr4:91830371..91830629 )

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]

rs7683787	NMD_transcript_variant; intron_variant; nc_transcript_variant	1(0/0/1)	0.804[CEU]