Hot Results
- Quick Search
- Large-scale studies
- Genome-wide Association Studies of ADHD
- Genome-wide Linkage Studies of ADHD
- Genome-wide CNV Analyses of ADHD
- Meta-analysis Studies of ADHD
- Data Summary
SNP Report
Basic Info
| Name | rs9898353 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:28451865(Fwd) | ||
| Variant Alleles | T/C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000589608; ENST00000584317; ENST00000394826; ENST00000584154; ENST00000475652) intron_variant(ENST00000584317; ENST00000247026; ENST00000540900; ENST00000589608; ENST00000583301; ENST00000580103; ENST00000584423; ENST00000479218; ENST00000577289; ENST00000394826; ENST00000584154; ENST00000475652; ENST00000588614; ENST00000581048; ENST00000585881; ENST00000467446; ENST00000581946) nc_transcript_variant(ENST00000540900; ENST00000583301; ENST00000577289; ENST00000581048; ENST00000467446; ENST00000581946) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.