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- Data Summary
SNP Report
Name | rs998850 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:50607388(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000444733) downstream_gene_variant(ENST00000432526; ENST00000420203) intron_variant(ENST00000357936; ENST00000431062; ENST00000444124; ENST00000444733; ENST00000426377; ENST00000380984; ENST00000430300; ENST00000454521; ENST00000489162) nc_transcript_variant(ENST00000454521; ENST00000489162) |
||
No. of Studies | 1 (significant: 1; non-significant: 0; 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.