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- Data Summary
SNP Report
Name | rs734252 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:91446472(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | 5_prime_UTR_variant; NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000559717; ENST00000558853; ENST00000558290) NMD_transcript_variant(ENST00000560451; ENST00000558161) intron_variant(ENST00000559999; ENST00000560451; ENST00000558161) nc_transcript_variant(ENST00000560534) non_coding_exon_variant(ENST00000560534) upstream_gene_variant(ENST00000360468; ENST00000558640; ENST00000561046; ENST00000559132; ENST00000560192; ENST00000557865; ENST00000559965; ENST00000431652; ENST00000560616) |
||
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.