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- Data Summary
SNP Report
Name | rs10228350 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:114060663(Fwd) | ||
Variant Alleles | A/T | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000412402; ENST00000440349; ENST00000441290) intron_variant(ENST00000412402; ENST00000440349; ENST00000441290; ENST00000324462; ENST00000393494; ENST00000350908; ENST00000495516; ENST00000462331; ENST00000408937; ENST00000393498; ENST00000393489; ENST00000459666; ENST00000378237; ENST00000403559; ENST00000393500) nc_transcript_variant(ENST00000495516; ENST00000459666) upstream_gene_variant(ENST00000415146) |
||
No. of Studies | 1 (significant: 0; non-significant: 1; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.