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- Data Summary
SNP Report
Name | rs10277729 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr12:21106269(Fwd); Chr2:199551733(Fwd); Chr3:105869587(Rev); Chr3:137375274(Fwd); Chr5:180318930(Fwd); Chr9:16225553(Fwd); ChrX:8743218(Fwd) | ||
Variant Alleles | T/C | ||
Functional Annotation | feature_elongation; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | feature_elongation(ENST00000357468; ENST00000380685; ENST00000380683) intron_variant(ENST00000440609; ENST00000357468; ENST00000380685; ENST00000380683; ENST00000381541; ENST00000553473; ENST00000554957; ENST00000540229) nc_transcript_variant(ENST00000440609) |
||
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.