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- Data Summary
SNP Report
Name | rs351770 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:112199199(Fwd) | ||
Variant Alleles | C/A | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000520401; ENST00000506997) intron_variant(ENST00000520401; ENST00000512790; ENST00000509024; ENST00000505459; ENST00000515755; ENST00000503445; ENST00000515463; ENST00000282999; ENST00000506997; ENST00000506987; ENST00000445150) nc_transcript_variant(ENST00000509024; ENST00000512790; ENST00000515755; ENST00000503445; ENST00000506987; ENST00000445150) upstream_gene_variant(ENST00000504696) |
||
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.