||chr10:62820815 - 62820815(1)
|Minor Allele Frequence
||intron_variant; non_coding_transcript_variant; upstream_gene_variant.
|Consequence to Transcript
||intron_variant(ENST00000493899); non_coding_transcript_variant(ENST00000493899); upstream_gene_variant(ENST00000242480, ENST00000411732, ENST00000439032, ENST00000637191, LRG_239t1)
|No. of Studies
||1 (Positive: 0; Negative: 1; Trend: 0)
|Overlap with SZ?
|Overlap with MDD?
SNP related studies (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
SNP related genes (count: 1)
Literature-origin SNPs (count: 0)
LD-proxies (count: 8)
Overlap with SZ from cross-disorder studies (count: 1)
|Kim, S. H.,2011
||For SZ, chi-square tests:allele, OR=0.979, X2=0.0268, P-value = 0.8698, P-value(permutation)=1;Fisher's exact test, genotype, X2=0.0339, P-value = 0.9832
||No significant association was observed.
Overlap with MDD from cross-disorder studies (count: 0)