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- Data Summary
SNP Report
Name | rs931908 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:4580832(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000575329) intron_variant(ENST00000574876; ENST00000573523; ENST00000575101; ENST00000575329; ENST00000572293; ENST00000570571; ENST00000269230; ENST00000570387; ENST00000441700; ENST00000436683; ENST00000301396) nc_transcript_variant(ENST00000573523; ENST00000441700) upstream_gene_variant(ENST00000575534; ENST00000573506; ENST00000573242) |
||
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.