ADHDgene Database

SNP Report

Basic Info

Name	rs9912741 dbSNP Ensembl
Location	Chr17:28359511(Fwd)
Variant Alleles	G/A
Ancestral Allele	A
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000423598; ENST00000440741) intron_variant(ENST00000419434; ENST00000440741; ENST00000394835; ENST00000588978; ENST00000423598; ENST00000536908; ENST00000584826; ENST00000320856; ENST00000378738; ENST00000394832; ENST00000541045) nc_transcript_variant(ENST00000584826)
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
EFCAB5	EF-hand calcium binding domain 5	17q11.2

SNPs in LD with rs9912741 (count: 6) View in gBrowse (chr17:28359511..28538532 )

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]

rs140701	intron_variant; upstream_gene_variant	3(1/2/0)	0.805[TSI]
rs1042173	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant	1(0/1/0)	0.961[CEU]; 0.847[GIH]; 0.955[MEX]; 0.932[TSI]
rs3813034	3_prime_UTR_variant; downstream_gene_variant	4(0/4/0)	0.961[CEU]; 0.866[GIH]; 0.912[MEX]; 0.954[TSI]
rs4325622	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	0.961[CEU]
rs1979572	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant	1(1/0/0)	0.923[CEU]
rs11080121	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	0.921[CEU]