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- Data Summary
SNP Report
Name | rs3765120 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:20852001(Fwd) | ||
Variant Alleles | A/T | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000515786) intron_variant(ENST00000447367; ENST00000382148; ENST00000382150; ENST00000382152; ENST00000413487; ENST00000509207; ENST00000382149; ENST00000515786; ENST00000359001) nc_transcript_variant(ENST00000382149; ENST00000515373) non_coding_exon_variant(ENST00000515373) |
||
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.