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- Data Summary
SNP Report
Name | rs1707988 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr3:39551526(Fwd) | ||
Variant Alleles | G/A/C | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000452959; ENST00000442631; ENST00000424090) intron_variant(ENST00000452959; ENST00000442631; ENST00000424090; ENST00000447324; ENST00000428261; ENST00000383754; ENST00000420739; ENST00000415443; ENST00000311042; ENST00000396228; ENST00000479860) nc_transcript_variant(ENST00000479860) |
||
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.