||chr10:62808178 - 62808178(1)
|Minor Allele Frequence
||3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant.
|Consequence to Transcript
||3_prime_UTR_variant(ENST00000373783); downstream_gene_variant(ENST00000242480, ENST00000411732, ENST00000439032); upstream_gene_variant(ENST00000425290)
|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: 2)
Literature-origin SNPs (count: 0)
LD-proxies (count: 4)
Overlap with SZ from cross-disorder studies (count: 1)
|Kim, S. H.,2011
||For SZ, chi-square tests:allele, OR=1.244, X2=3.3587, P-value = 0.0668, P-value(permutation)=0.305;Fisher's exact test, genotype, X2=5.4069, P-value = 0.067
||No significant association was observed.
Overlap with MDD from cross-disorder studies (count: 0)