- 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
Name | rs4485648 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr22:19919405(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000400518; ENST00000400519; ENST00000400521; ENST00000400525; ENST00000474308; ENST00000334363; ENST00000542719; ENST00000535882; ENST00000496729; ENST00000491939) nc_transcript_variant(ENST00000474308; ENST00000491939; ENST00000496729) |
||
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.