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- Data Summary
SNP Report
Name | rs772175 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr2:96944553(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000429650) downstream_gene_variant(ENST00000480242; ENST00000493271) intron_variant(ENST00000349783) nc_transcript_variant(ENST00000484372; ENST00000497539) non_coding_exon_variant(ENST00000484372; ENST00000497539) synonymous_variant(ENST00000429650; ENST00000323853) upstream_gene_variant(ENST00000480835) |
||
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.