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- Data Summary
SNP Report
Name | rs172424 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:18022950(Fwd) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000525422; ENST00000527494; ENST00000530925; ENST00000524716; ENST00000533328) intron_variant(ENST00000525422; ENST00000527494; ENST00000265965; ENST00000528200; ENST00000532389; ENST00000530925; ENST00000529728; ENST00000530613; ENST00000524716; ENST00000525920; ENST00000525523; ENST00000533328; ENST00000532265; ENST00000532212) nc_transcript_variant(ENST00000525523; ENST00000532212) upstream_gene_variant(ENST00000529151) |
||
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.