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- Data Summary
SNP Report
Name | rs7688805 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:20732334(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000506702; ENST00000467997; ENST00000471979; ENST00000515786) downstream_gene_variant(ENST00000502374; ENST00000513459; ENST00000508952; ENST00000506648; ENST00000502938; ENST00000538990; ENST00000503585; ENST00000295290; ENST00000444671; ENST00000360916) intron_variant(ENST00000506702; ENST00000467997; ENST00000471979; ENST00000507634; ENST00000382148; ENST00000447367; ENST00000382150; ENST00000382152; ENST00000413487; ENST00000382149; ENST00000509207; ENST00000515786; ENST00000359001) nc_transcript_variant(ENST00000382149) |
||
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.