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SNP Report
Name | rs3793227 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:159093237 - 159093237(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.124201 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000262178, ENST00000377633, ENST00000402066) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; 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 > 0.05, genotype P-value > 0.05 in all model | No significant association was observed. | Negative |