- 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 | rs497993 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:27895528(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | 5_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; splice_donor_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000583940; ENST00000582829) downstream_gene_variant(ENST00000394869; ENST00000578073; ENST00000473217; ENST00000584522; ENST00000225394) intron_variant(ENST00000581474) nc_transcript_variant(ENST00000581474) splice_donor_variant(ENST00000580183; ENST00000578749) upstream_gene_variant(ENST00000581411; ENST00000579050; ENST00000580132; ENST00000307201; ENST00000577934; ENST00000301057; ENST00000378818; ENST00000579674) |
||
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.