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- Data Summary
SNP Report
Name | rs903502 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:37829604(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000577337) downstream_gene_variant(ENST00000582276; ENST00000584620; ENST00000580898; ENST00000581428; ENST00000394246; ENST00000269582) intron_variant(ENST00000577337; ENST00000429199; ENST00000378011; ENST00000579146; ENST00000309862; ENST00000300658) nc_transcript_variant(ENST00000309862) |
||
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.