ADHDgene Database

SNP Report

Basic Info

Name	rs237895 dbSNP Ensembl
Location	Chr3:8807423(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000431493; ENST00000474615; ENST00000449615) intron_variant(ENST00000472766; ENST00000316793) nc_transcript_variant(ENST00000472766)
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
Park J, 2010	C/T	C	TDT P-value=0.64, OR=1.13, 95% CI=0.78-1.64. TDT P-value=0.64, OR=1.13, 95% CI=0.78-1.64.	TDT analysis did not demonstrate significant association of ...... TDT analysis did not demonstrate significant association of this SNP with ADHD. But an association with social cognitive impairments in a subset of the ADHD probands (N=112) was found for this SNP (F=3.09, P-value=0.05). More...	Non-significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
OXTR	oxytocin receptor	3p25	1(0/1/0)

Approved Symbol	Approved Name	Location
CAV3	caveolin 3	3p25

SNPs in LD with rs237895 (count: 1) View in gBrowse (chr3:8807423..8808285 )

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