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- Data Summary
SNP Report
Name | rs12475068 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr2:234622110(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000446481; ENST00000484784) intron_variant(ENST00000373445; ENST00000344644; ENST00000373450; ENST00000354728; ENST00000446481; ENST00000373424; ENST00000480628; ENST00000373426; ENST00000305139; ENST00000484784; ENST00000406651) missense_variant(ENST00000373414) nc_transcript_variant(ENST00000480628; ENST00000478062) non_coding_exon_variant(ENST00000478062) upstream_gene_variant(ENST00000439336) |
||
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.