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- Data Summary
SNP Report
Name | rs11659017 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:79018379(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000572329; ENST00000575750) intron_variant(ENST00000575989; ENST00000570913; ENST00000572329; ENST00000575712; ENST00000321280; ENST00000575750; ENST00000576470; ENST00000428708; ENST00000575245; ENST00000321300; ENST00000435091; ENST00000392411; ENST00000571530; ENST00000573894) nc_transcript_variant(ENST00000570913; ENST00000576470; 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.