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- Data Summary
SNP Report
Name | rs866006 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:112176559(Fwd) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; synonymous_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000508624) NMD_transcript_variant(ENST00000508624; ENST00000520401) downstream_gene_variant(ENST00000507379; ENST00000512211; ENST00000514164; ENST00000502371) intron_variant(ENST00000520401) synonymous_variant(ENST00000257430; ENST00000508376; ENST00000457016; LRG_130_t1; LRG_130_t2; LRG_130_t3) |
||
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.