- 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 | rs6505162 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:28444183(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Functional Annotation | 5_prime_UTR_variant; NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000585881) NMD_transcript_variant(ENST00000584317; ENST00000475652; ENST00000394826; ENST00000584154) intron_variant(ENST00000584317; ENST00000475652; ENST00000479218; ENST00000583301; ENST00000394826; ENST00000582938; ENST00000540900; ENST00000577289; ENST00000584423; ENST00000247026; ENST00000584154) nc_transcript_variant(ENST00000583301; ENST00000467446; ENST00000582938; ENST00000540900; ENST00000577289; ENST00000362201; ENST00000586878) non_coding_exon_variant(ENST00000467446; ENST00000362201; ENST00000586878) upstream_gene_variant(ENST00000581048; ENST00000580103; ENST00000589608; ENST00000588614) |
||
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.