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SNP Report
Name | rs17452383 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:13388824 - 13388824(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.0828674 | ||
Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000278174, ENST00000527102, ENST00000528120, ENST00000530907); downstream_gene_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403482, ENST00000403510, ENST00000472842, ENST00000524392); NMD_transcript_variant(ENST00000527102) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | YES |
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 |
---|---|---|---|
Soria, V.,2010 | X2-tests:allele P-value = 0.938, Model Recessive, genotype P-value = 0.035, OR(95%CI)=3.00 (1.03-8.77) | Significant association was found. | Positive |