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- Data Summary
SNP Report
Name | rs7216631 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:28495112(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000584317; ENST00000584154; ENST00000475652; ENST00000394826; ENST00000589608) intron_variant(ENST00000588614; ENST00000580103; ENST00000247026; ENST00000467446; ENST00000584317; ENST00000585881; ENST00000540900; ENST00000584154; ENST00000475652; ENST00000577289; ENST00000581048; ENST00000394826; ENST00000589608) nc_transcript_variant(ENST00000467446; ENST00000540900; ENST00000581048; ENST00000577289) |
||
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.