ADHDgene Database

SNP Report

Basic Info

Name	rs6027437 dbSNP Ensembl
Location	Chr20:58816388(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000431181; ENST00000437035; ENST00000458422; ENST00000432910; ENST00000421257; ENST00000427820) nc_transcript_variant(ENST00000431181; ENST00000437035; ENST00000458422; ENST00000432910; ENST00000421257; ENST00000427820)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs6027437 (count: 4) View in gBrowse (chr20:58799401..58816388 )

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]

rs6100796	intron_variant; nc_transcript_variant	1(0/0/1)	0.943[CEU]; 0.898[MEX]; 0.879[TSI]
rs1535028	intron_variant; nc_transcript_variant	1(0/0/1)	0.838[CHD]; 0.822[JPT]; 0.902[MEX]
rs2865793	intron_variant; nc_transcript_variant	1(0/0/1)	0.943[CEU]; 0.853[JPT]; 0.948[MEX]; 0.874[TSI]
rs7271202	intron_variant; nc_transcript_variant	1(0/0/1)	0.943[CEU]; 0.948[MEX]; 0.879[TSI]