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- Data Summary
SNP Report
Name | rs324389 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:34777714(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000396095; ENST00000381544) intron_variant(ENST00000419766; ENST00000439852; ENST00000358772; ENST00000436945; ENST00000539747; ENST00000428922; ENST00000431669; ENST00000537560; ENST00000360581; ENST00000442669; ENST00000396095; ENST00000544556; ENST00000381542; ENST00000535640; ENST00000531252; ENST00000359791; ENST00000381544; ENST00000381553; ENST00000381539) nc_transcript_variant(ENST00000419766; ENST00000439852; ENST00000358772; ENST00000436945; ENST00000539747; ENST00000428922; ENST00000431669; ENST00000537560; ENST00000442669; ENST00000544556; ENST00000535640) |
||
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.