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- Data Summary
SNP Report
Name | rs925533 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr1:202534108(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000466273) intron_variant(ENST00000406302; ENST00000391959; ENST00000367270; ENST00000491336; ENST00000336894; ENST00000367269; ENST00000290419) nc_transcript_variant(ENST00000290419; ENST00000491336; ENST00000367269) upstream_gene_variant(ENST00000465284; ENST00000462074) |
||
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.