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- Data Summary
SNP Report
Name | rs2073950 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr12:111894072(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000483311) downstream_gene_variant(ENST00000341259) intron_variant(ENST00000468920; ENST00000550889; ENST00000377617; ENST00000389153; ENST00000542287; ENST00000535949; ENST00000551551; ENST00000482777; ENST00000389154; ENST00000550844; ENST00000483311; ENST00000550104) nc_transcript_variant(ENST00000468920; ENST00000551551) upstream_gene_variant(ENST00000484991; ENST00000475132) |
||
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.