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- Data Summary
SNP Report
Name | rs17136314 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:3357881(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000571101; ENST00000293995; ENST00000573594; ENST00000498240; ENST00000574298) nc_transcript_variant(ENST00000575234; ENST00000498240; ENST00000574245; ENST00000571101) non_coding_exon_variant(ENST00000575234; ENST00000574245) upstream_gene_variant(ENST00000575812; ENST00000573608; ENST00000571388; ENST00000573695; ENST00000574598; ENST00000576104; ENST00000570634; ENST00000572297; ENST00000396862; ENST00000572999; ENST00000573828; ENST00000571748) |
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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.