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- Data Summary
SNP Report
Name | rs501250 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:112155793(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000508624) intron_variant(ENST00000257430; ENST00000507379; ENST00000508624; ENST00000512211; ENST00000457016; ENST00000508376; ENST00000506342; LRG_130_t2; LRG_130_t1; LRG_130_t3) nc_transcript_variant(ENST00000506342) upstream_gene_variant(ENST00000504915; ENST00000502371) |
||
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.