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- Data Summary
SNP Report
Name | rs430665 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:112228667(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000511865) downstream_gene_variant(ENST00000506997; ENST00000503445; ENST00000509024) intron_variant(ENST00000497856; ENST00000379638; ENST00000504247; ENST00000261482; ENST00000513339; ENST00000545426; ENST00000511865; ENST00000474542) missense_variant(ENST00000391338) nc_transcript_variant(ENST00000512790; ENST00000497856; ENST00000474542) non_coding_exon_variant(ENST00000512790) |
||
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.