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- Data Summary
SNP Report
Name | rs4773 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:91463842(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000560451; ENST00000360468; ENST00000559717; ENST00000558161) NMD_transcript_variant(ENST00000560451; ENST00000558161; ENST00000559704) downstream_gene_variant(ENST00000430376; ENST00000558538; ENST00000431652; ENST00000560147; ENST00000559558; ENST00000558374; ENST00000559341; ENST00000560926; ENST00000560880; ENST00000561448; ENST00000557865; ENST00000557990) intron_variant(ENST00000559704) nc_transcript_variant(ENST00000560522) non_coding_exon_variant(ENST00000560522) |
||
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.