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SNP Report
Name | rs11191580 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:103146454 - 103146454(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.146965 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000343289, ENST00000369857, ENST00000404739, ENST00000452156, ENST00000461461, ENST00000470299); NMD_transcript_variant(ENST00000452156, ENST00000461461); non_coding_transcript_variant(ENST00000369857) | ||
No. of Studies | 3 (Positive: 3; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Hamshere, M. L.,2012 | Association analysis:OR=1.19, P-value = 0.01 | Significant association was observed in SZ. | Positive association was observed in SZ. |
Andreassen OA, 2013 | Conditional FDR; SCZ loci given BD: P-value=0.00000171, FDR=0.049, FDR=0.005 for SCZ and BD | To estimate the number of independent loci, we 'pruned' the associated SNPs (removed SNPs with linkage disequilibrium (LD)>0.2), and identified a total of 58 independent loci with a significance threshold of conditional FDR<0.32. | Positive |