Hot Results
Quick Search
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 | rs12376892 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr9:119348005(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | intron_variant(ENST00000288520; ENST00000373986; ENST00000341734; ENST00000361209; ENST00000361477; ENST00000313400; ENST00000373996) nc_transcript_variant(ENST00000423715) non_coding_exon_variant(ENST00000423715) |
||
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.