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- Data Summary
SNP Report
Name | rs607138 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr6:16749567(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000479680) intron_variant(ENST00000483591; ENST00000244769; ENST00000473388; ENST00000495178; ENST00000467008; ENST00000492857; ENST00000483954; ENST00000498374; ENST00000296858; ENST00000436367; ENST00000344707; ENST00000450222) nc_transcript_variant(ENST00000483591; ENST00000473388; ENST00000495178; ENST00000467008; ENST00000492857; ENST00000483954; ENST00000498374) |
||
No. of Studies | 1 (significant: 0; non-significant: 0; trend: 1) | ||
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.