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- Data Summary
SNP Report
Name | rs7657608 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:168154181(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000511905; ENST00000507370; ENST00000502821; ENST00000505187; ENST00000515143; ENST00000511226; ENST00000502741; ENST00000507086; ENST00000515316) intron_variant(ENST00000357154; ENST00000504953; ENST00000357545; ENST00000511531; ENST00000502330; ENST00000506886; ENST00000510741; ENST00000511905; ENST00000507370; ENST00000511269; ENST00000512681; ENST00000502821; ENST00000505187; ENST00000512648; ENST00000510403; ENST00000515143; ENST00000511226; ENST00000502741; ENST00000509854; ENST00000507086; ENST00000515316; ENST00000541637; ENST00000506697; ENST00000512042; ENST00000534949; ENST00000535728; ENST00000421836; ENST00000541354) |
||
No. of Studies | 2 (significant: 0; non-significant: 2; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.