ADHDgene Database

SNP Report

Basic Info

Name	rs2303940 dbSNP Ensembl
Location	Chr7:150773165(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000460010; ENST00000461979; ENST00000472204; ENST00000540185; ENST00000469355; ENST00000297532; ENST00000482697; ENST00000478477; ENST00000467237; ENST00000469237; ENST00000465272; ENST00000480107; ENST00000496663; ENST00000478883; ENST00000483105; ENST00000493040; ENST00000466855; ENST00000353841; ENST00000460980; ENST00000483953; ENST00000489884; ENST00000494298; ENST00000482806; ENST00000482571; ENST00000459800) nc_transcript_variant(ENST00000485974; ENST00000469467) non_coding_exon_variant(ENST00000485974; ENST00000469467) synonymous_variant(ENST00000413384; ENST00000392826; ENST00000310317; ENST00000461735; ENST00000485713)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location
SLC4A2	solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane protein band 3-like 1)	7q35-q36
LOC100996677	uncharacterized LOC100996677 [MODEL Refseq, protein coding]	7
FASTK	Fas-activated serine/threonine kinase	7q35

SNPs in LD with rs2303940 (count: 1) View in gBrowse (chr7:150773165..150774308 )

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]

rs2288648	3_prime_UTR_variant; downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant	1(0/1/0)	1.0[CHB]; 1.0[CHD]; 0.849[JPT]; 1.0[MEX]; 0.848[YRI]