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SNP Report
Name | rs7192086 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:12967754 - 12967754(1) | ||
Variant Alleles | T/A | ||
Ancestral Allele | A | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.258187 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000558583) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; 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 |
---|---|---|---|
Schanze, D.,2011 | X2 tests:allele P-value = 0.78 for SCZ. | No significant association was observed. | Negative |