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- Data Summary
SNP Report
Name | rs9265 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr22:19957631(Fwd) | ||
Variant Alleles | C/A | ||
Ancestral Allele | C | ||
Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000344269; ENST00000263207) downstream_gene_variant(ENST00000406520; ENST00000403184; ENST00000207636; ENST00000449653; ENST00000403710; ENST00000401994; ENST00000407537; ENST00000480792; ENST00000406522; ENST00000361682; ENST00000406259; ENST00000428707; ENST00000412786) nc_transcript_variant(ENST00000495096) non_coding_exon_variant(ENST00000495096) |
||
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.