ADHDgene Database

SNP Report

Basic Info

Name	rs10066070 dbSNP Ensembl
Location	Chr5:94093011(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000515393; ENST00000514040; ENST00000312216; ENST00000429576; ENST00000508509; ENST00000505078; ENST00000573031; ENST00000573439; ENST00000573142; ENST00000577136; ENST00000575480; ENST00000574707) nc_transcript_variant(ENST00000514040; ENST00000573031)
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)
MCTP1	multiple C2 domains, transmembrane 1	5q15	1(0/1/0)

SNPs in LD with rs10066070 (count: 1) View in gBrowse (chr5:94093011..94141447 )

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]

rs11953346	intron_variant	1(0/1/0)	0.959[CEU]; 1.0[CHB]; 0.968[GIH]; 1.0[MEX]; 0.859[MKK]; 0.899[TSI]