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SNP Report
Name | rs11921360 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:119893208 - 119893208(1) | ||
Variant Alleles | C/A | ||
Ancestral Allele | A | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.234824 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000264235, ENST00000316626) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | YES |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Saus, E.,2010 | association analyses with diagnosis:codominant P-value = 0.097, dominant P-value = 0.038, recessive P-value = 0.223, additive P-value = 0.033, all P-value > 0.05 after multiple testing correction. | No significant association was observed. | Negative |