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- Data Summary
SNP Report
Name | rs4969377 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:79053078(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000572329; ENST00000575750; ENST00000574804) downstream_gene_variant(ENST00000570913) intron_variant(ENST00000321280; ENST00000572329; ENST00000576470; ENST00000575712; ENST00000428708; ENST00000575989; ENST00000575750; ENST00000435091; ENST00000575245; ENST00000576364; ENST00000572918; ENST00000575958; ENST00000573894; ENST00000572073; ENST00000571530; ENST00000321300; ENST00000573659; ENST00000392411; ENST00000573017; ENST00000573677; ENST00000574804) nc_transcript_variant(ENST00000576470; ENST00000576364; ENST00000573894; ENST00000573017) upstream_gene_variant(ENST00000577097; ENST00000574688) |
||
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.