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- Data Summary
SNP Report
Name | rs4969387 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:79081724(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000572329) downstream_gene_variant(ENST00000576756; ENST00000574804; ENST00000573677; ENST00000572073; ENST00000574027; ENST00000577097) intron_variant(ENST00000321280; ENST00000428708; ENST00000572329; ENST00000435091; ENST00000575712; ENST00000575245; ENST00000416299; ENST00000572498; ENST00000576225; ENST00000392411; ENST00000575841; ENST00000321300) nc_transcript_variant(ENST00000576225; ENST00000576995) non_coding_exon_variant(ENST00000576995) |
||
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.