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- Data Summary
SNP Report
Name | rs6858749 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:56290437(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000508404) downstream_gene_variant(ENST00000309964) intron_variant(ENST00000506103; ENST00000381334; ENST00000508404; ENST00000506198; ENST00000509575; ENST00000542052; ENST00000514904; ENST00000508561) nc_transcript_variant(ENST00000515591; ENST00000506103; ENST00000509575; ENST00000514904; ENST00000508561) non_coding_exon_variant(ENST00000515591) |
||
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.