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- Data Summary
SNP Report
Name | rs174534 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:61549458(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000536352; ENST00000327797) intron_variant(ENST00000535042; ENST00000389602; ENST00000265460; ENST00000546247; ENST00000278836) nc_transcript_variant(ENST00000535042; ENST00000539361; ENST00000546247; ENST00000537318) non_coding_exon_variant(ENST00000539361; ENST00000537318) |
||
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.