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- Data Summary
SNP Report
Name | rs211141 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:17994314(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000527494; ENST00000525422; ENST00000532546) intron_variant(ENST00000527494; ENST00000525422; ENST00000265965; ENST00000529440; ENST00000529151; ENST00000528200; ENST00000532546; ENST00000533241; ENST00000525920; ENST00000532265; ENST00000529728) nc_transcript_variant(ENST00000529440) |
||
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.