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- Data Summary
SNP Report
Name | rs174555 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:61579760(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000424501) downstream_gene_variant(ENST00000545986; ENST00000448607; ENST00000473263; ENST00000541683; ENST00000410394; ENST00000539419) intron_variant(ENST00000574708; ENST00000542506; ENST00000433932; ENST00000496123; ENST00000540767; ENST00000545405; ENST00000545245; ENST00000424501; ENST00000491310; ENST00000544309; ENST00000544696; ENST00000466716; ENST00000350997; ENST00000421879) nc_transcript_variant(ENST00000496123) upstream_gene_variant(ENST00000522639; ENST00000257261; ENST00000522056; ENST00000517839; ENST00000539999) |
||
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.