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- Data Summary
SNP Report
Name | rs550818 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:27901975(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000578670) downstream_gene_variant(ENST00000581925; ENST00000378818; ENST00000579050; ENST00000585148; ENST00000301057; ENST00000579674; ENST00000491377; ENST00000578266; ENST00000586574; ENST00000582829; ENST00000581411; ENST00000577934; ENST00000580183; ENST00000583940; ENST00000578749) intron_variant(ENST00000225394; ENST00000578670; ENST00000581474; ENST00000581348; ENST00000473217; ENST00000394869) missense_variant(ENST00000579937) nc_transcript_variant(ENST00000581474; ENST00000473217) |
||
No. of Studies | 2 (significant: 1; non-significant: 1; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.