ADHDgene Database

SNP Report

Basic Info

Name	rs10005756 dbSNP Ensembl
Location	Chr4:62800350(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000512091; ENST00000514591; ENST00000509896; ENST00000511324; ENST00000507164; ENST00000506700; ENST00000508693; ENST00000514157; ENST00000507625; ENST00000508946; ENST00000504896; ENST00000506720; ENST00000502815; ENST00000506746; ENST00000514996; ENST00000508078; ENST00000545650) nc_transcript_variant(ENST00000508078)
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)
LPHN3	latrophilin 3	4q13.1	4(3/0/1)

SNPs in LD with rs10005756 (count: 1) View in gBrowse (chr4:62800350..62800626 )

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]

rs10013832	nc_transcript_variant; non_coding_exon_variant; synonymous_variant	1(0/0/1)	1.0[YRI]