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- Data Summary
SNP Report
Name | rs3008354 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr10:135120646(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000482278) intron_variant(ENST00000487796; ENST00000482278; ENST00000417178; ENST00000480198; ENST00000470829; ENST00000368563) nc_transcript_variant(ENST00000487796; ENST00000480198; ENST00000470829) upstream_gene_variant(ENST00000252936; ENST00000368554; ENST00000543663; ENST00000361518; ENST00000359035; ENST00000482153; ENST00000463816) |
||
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.