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- Data Summary
SNP Report
Name | rs6744132 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr2:239144542(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000409356; ENST00000409574; ENST00000417803; ENST00000409182; ENST00000436051; ENST00000409002; ENST00000409160; ENST00000272937; ENST00000450098) intron_variant(ENST00000456601; ENST00000438457) nc_transcript_variant(ENST00000456601; ENST00000438457) upstream_gene_variant(ENST00000475669; ENST00000409942; ENST00000409070; ENST00000409376; ENST00000466075; ENST00000334973; ENST00000470346) |
||
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.