ADHDgene Database

SNP Report

Basic Info

Name	rs1997205 dbSNP Ensembl
Location	Chr12:102046394(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000361685; ENST00000361466; ENST00000550270; ENST00000452455; ENST00000551300; ENST00000441232; ENST00000541119; ENST00000547509; ENST00000553190; ENST00000536007; ENST00000545503; ENST00000392934; ENST00000550501; ENST00000549145; ENST00000547405; ENST00000360610; ENST00000547027) nc_transcript_variant(ENST00000550501; ENST00000547027) upstream_gene_variant(ENST00000552081)
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)
MYBPC1	myosin binding protein C, slow type	12q32	1(0/1/0)

SNPs in LD with rs1997205 (count: 1) View in gBrowse (chr12:102022264..102046394 )

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]

rs17031719	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	0.838[CHB]; 1.0[JPT]