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- Data Summary
SNP Report
Name | rs6501169 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:3353205(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000574245; ENST00000574674; ENST00000575332) intron_variant(ENST00000574598; ENST00000573695; ENST00000572297; ENST00000576104; ENST00000570634; ENST00000396862; ENST00000571748; ENST00000573608) nc_transcript_variant(ENST00000574598; ENST00000571748; ENST00000573695; ENST00000572297; ENST00000576104; ENST00000570634) upstream_gene_variant(ENST00000571101; ENST00000268674; ENST00000573594; ENST00000498240; ENST00000574298; ENST00000575234; ENST00000293995) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.