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- Data Summary
SNP Report
Name | rs2920781 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:43924682(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000419262; ENST00000433380; ENST00000450810) intron_variant(ENST00000472960; ENST00000354127; ENST00000419262; ENST00000299989; ENST00000381761; ENST00000541030; ENST00000396879; ENST00000355438; ENST00000321596; ENST00000433380; ENST00000450810; ENST00000396923) nc_transcript_variant(ENST00000472960; ENST00000469461) non_coding_exon_variant(ENST00000469461) |
||
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.