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- Data Summary
SNP Report
Name | rs790939 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr13:50660881(Fwd) | ||
Variant Alleles | T/A | ||
Ancestral Allele | T | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000478860) intron_variant(ENST00000469754; ENST00000486895; ENST00000425586; ENST00000463474; ENST00000378180; ENST00000461527; ENST00000468168; ENST00000491341; ENST00000476738; ENST00000468522; ENST00000490577; ENST00000467721; ENST00000491615) nc_transcript_variant(ENST00000469754; ENST00000486895; ENST00000425586; ENST00000463474; ENST00000461527; ENST00000468168; ENST00000491341; ENST00000476738; ENST00000468522; ENST00000490577; ENST00000467721; ENST00000491615) upstream_gene_variant(ENST00000438752; ENST00000421758; ENST00000458725; ENST00000443587; ENST00000416253; ENST00000449579; ENST00000433070; ENST00000235290) |
||
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.