ADHDgene Database

SNP Report

Basic Info

Name	rs9291413 dbSNP Ensembl
Location	Chr4:20861032(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000515786) intron_variant(ENST00000382148; ENST00000447367; ENST00000382150; ENST00000413487; ENST00000382152; ENST00000509207; ENST00000515786; ENST00000382149; ENST00000359001; ENST00000515373) nc_transcript_variant(ENST00000382149; ENST00000515373)
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)
KCNIP4	Kv channel interacting protein 4	4p15.32	1(1/0/0)

SNPs in LD with rs9291413 (count: 1) View in gBrowse (chr4:20851050..20861032 )

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]

rs4697192	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant	1(1/0/0)	0.905[CHB]; 0.85[JPT]