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Large-scale studies
- Genome-wide Association Studies of ADHD
- Genome-wide Linkage Studies of ADHD
- Genome-wide CNV Analyses of ADHD
- Meta-analysis Studies of ADHD
Data Summary
SNP Report
Name | rs10150332 dbSNP Ensembl | ||
---|---|---|---|
Location | chr14:79936964(Fwd) | ||
Variant Alleles | T/C | ||
Functional Annotation | intron_variant; nc_transcript_variant; NMD_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000281127; ENST00000335750; ENST00000428277; ENST00000553803; ENST00000554719; ENST00000554738; ENST00000555073; ENST00000555387; ENST00000556003; ENST00000557594) nc_transcript_variant(ENST00000553803; ENST00000555073; ENST00000556003) NMD_transcript_variant(ENST00000554738; ENST00000555387) |
||
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.