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- Data Summary
SNP Report
Name | rs17652121 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:44073973(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant. | ||
Consequence to Transcript | nc_transcript_variant(ENST00000570299) non_coding_exon_variant(ENST00000570299) synonymous_variant(ENST00000420682; ENST00000415613; ENST00000446361; ENST00000334239; ENST00000571987; ENST00000340799; ENST00000576518; ENST00000535772; ENST00000344290; ENST00000431008; ENST00000574436; ENST00000351559; ENST00000262410; ENST00000347967) upstream_gene_variant(ENST00000537309) |
||
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.