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- Data Summary
SNP Report
Name | rs4969349 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:79006033(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | nc_transcript_variant(ENST00000577066; ENST00000573167) non_coding_exon_variant(ENST00000577066; ENST00000573167) upstream_gene_variant(ENST00000572329; ENST00000575750; ENST00000428708; ENST00000575712; ENST00000542745; ENST00000321280; ENST00000570913; ENST00000575989; ENST00000576470; ENST00000321300; ENST00000435091; ENST00000575245; ENST00000392411; ENST00000571530; ENST00000573894) |
||
No. of Studies | 1 (significant: 0; non-significant: 1; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.