ADHDgene Database

SNP Report

Basic Info

Name	rs13317247 dbSNP Ensembl
Location	chr3:7026535(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000357716; ENST00000389335; ENST00000389336; ENST00000402647; ENST00000403881; ENST00000435689; ENST00000440923; ENST00000443259; ENST00000448328; ENST00000467425; ENST00000486284) NMD_transcript_variant(ENST00000389335; ENST00000435689; ENST00000440923; ENST00000443259; ENST00000467425)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Yang L, 2013			P-value=0.0000637 P-value=0.0000637	The SNPs associated with P values of 1E-5 or lower The SNPs associated with P values of 1E-5 or lower	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
GRM7	glutamate receptor, metabotropic 7	3p26-p25	3(2/1/0)

SNPs in LD with rs13317247 (count: 1) View in gBrowse (chr3:7026273..7026535 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.