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- Data Summary
SNP Report
Name | rs1266483 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:91462406(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000559704; ENST00000561448; ENST00000560451; ENST00000558161) downstream_gene_variant(ENST00000560522; ENST00000560147; ENST00000560880) intron_variant(ENST00000559704; ENST00000561448; ENST00000560451; ENST00000430376; ENST00000558538; ENST00000557990; ENST00000557865; ENST00000560926; ENST00000558374; ENST00000360468; ENST00000558161; ENST00000559558; ENST00000431652; ENST00000559717; ENST00000559341) nc_transcript_variant(ENST00000558538; ENST00000560926; ENST00000558374; ENST00000559558; ENST00000559341) |
||
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.