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- Data Summary
SNP Report
Name | rs10938813 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:115899782(Fwd); Chr11:133365486(Rev); Chr13:51323762(Rev); Chr17:78690055(Rev); Chr4:10799734(Fwd); Chr7:102445452(Fwd) | ||
Variant Alleles | G/A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000420217; ENST00000442873; ENST00000574767) intron_variant(ENST00000524381; ENST00000529038; ENST00000420217; ENST00000413034; ENST00000409231; ENST00000442873; ENST00000574767; ENST00000570891; ENST00000306801; ENST00000577161; ENST00000544334; ENST00000537330; ENST00000572733; ENST00000400393) nc_transcript_variant(ENST00000529038; ENST00000577161; ENST00000572733) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
SNPs in LD with rs10938813 (count: 1) View in gBrowse (chr11; 11; 13; 17; 4; 7:20851050..115899782 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.