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- Data Summary
SNP Report
Name | rs819268 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:56235931(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000264228; ENST00000505210; ENST00000510637; ENST00000595103; ENST00000598906; ENST00000514398; ENST00000596289; ENST00000596312; ENST00000433175; ENST00000595734) nc_transcript_variant(ENST00000510637; ENST00000596312; ENST00000595103; ENST00000514398; ENST00000598906; ENST00000596289; ENST00000433175; ENST00000595734) |
||
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.