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- Data Summary
SNP Report
Name | rs9972882 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:37807698(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000578577) intron_variant(ENST00000578254; ENST00000577248; ENST00000578232; ENST00000585214; ENST00000580611; ENST00000544210; ENST00000579479; ENST00000583582; ENST00000394250; ENST00000581894; ENST00000578577; ENST00000580551; ENST00000583718; ENST00000336308) nc_transcript_variant(ENST00000578232; ENST00000578254; ENST00000585214; ENST00000583582; ENST00000580551) upstream_gene_variant(ENST00000580331; ENST00000443521; ENST00000583419; ENST00000460894; ENST00000484773; ENST00000488876; ENST00000582874) |
||
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.