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- Data Summary
SNP Report
Basic Info
| Name | rs7140561 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr14:39736680(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | 5_prime_UTR_variant; intron_variant; missense_variant; nc_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158) SIFT Annotation: tolerated(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158) |
||
| Consequence to Transcript | 5_prime_UTR_variant(ENST00000556148) intron_variant(ENST00000341749; ENST00000396165; ENST00000553728; ENST00000554392; ENST00000555716; ENST00000556990; ENST00000557038; ENST00000603904) missense_variant(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158) nc_transcript_variant(ENST00000556990) upstream_gene_variant(ENST00000553520; ENST00000605298) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
