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- Data Summary
SNP Report
Name | rs11030101 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:27680744(Fwd) | ||
Variant Alleles | A/T | ||
Ancestral Allele | A | ||
Functional Annotation | 5_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000525528; ENST00000439476) NMD_transcript_variant(ENST00000530786) downstream_gene_variant(ENST00000532965) intron_variant(ENST00000395986; ENST00000356660; ENST00000584049; ENST00000533246; ENST00000530786; ENST00000530861; ENST00000395978; ENST00000395983; ENST00000533131; ENST00000438929; ENST00000525950; ENST00000532997; ENST00000395981; ENST00000418212; ENST00000314915; ENST00000420794; ENST00000395980) nc_transcript_variant(ENST00000530686; ENST00000500662; ENST00000499008; ENST00000501176; ENST00000502161; ENST00000499568; ENST00000530313; ENST00000584049) non_coding_exon_variant(ENST00000499568; ENST00000530686; ENST00000500662; ENST00000499008; ENST00000501176; ENST00000502161; ENST00000530313) upstream_gene_variant(ENST00000528035) |
||
No. of Studies | 1 (significant: 1; non-significant: 0; 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.