||chr10:67906841 - 67906841(1)
|Minor Allele Frequence
||non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
|Consequence to Transcript
||non_coding_transcript_exon_variant(ENST00000473922); non_coding_transcript_variant(ENST00000473922); synonymous_variant(ENST00000212015, ENST00000403579, ENST00000406900, ENST00000432464)
|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: 14)
Overlap with SZ from cross-disorder studies (count: 1)
||For SZ, X2 test:genotype, X2(2df)=0.0744, P-value = 0.963;allele, X2(2df)=0.0644, P-value = 0.8
||No significant association was observed.
Overlap with MDD from cross-disorder studies (count: 0)