ADHDgene Database

SNP Report

Basic Info

Name	rs4765905 dbSNP Ensembl
Location	Chr12:2349584(Fwd)
Variant Alleles	G/C
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000335762; ENST00000399655; ENST00000399644; ENST00000399595; ENST00000480911; ENST00000399597; ENST00000399638; ENST00000399621; ENST00000399637; ENST00000399641; ENST00000399591; ENST00000347598; ENST00000399606; ENST00000399601; ENST00000327702; ENST00000399629; ENST00000344100; ENST00000399649; ENST00000399603; ENST00000399634; ENST00000399617; ENST00000402845; ENST00000406454; LRG_334_t1; LRG_334_t4; LRG_334_t3; LRG_334_t2)
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)
CACNA1C	calcium channel, voltage-dependent, L type, alpha 1C subunit	12p13.3	1(0/1/0)

SNPs in LD with rs4765905 (count: 1) View in gBrowse (chr12:2345295..2349584 )

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]

rs1006737	intron_variant	1(0/1/0)	1.0[ASW]; 1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 0.955[LWK]; 1.0[MEX]; 0.954[MKK]; 0.968[TSI]; 0.924[YRI]