Identification of <i>VIPR2</i> rare and common variants in the Chinese Han population with schizophrenia.

Front Mol Neurosci · 2023 · PMC10174236 · PMID 37181653

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nominally significantno p-value reported

Additionally, there was a nominally significant association between SCZ and the rare non-synonymous variant rs199630455 ( P allele = 0.009, P genotype = 0.009, OR for “C” [95% CI] = 0.206 [0.054 ~ 0.778]), and the alter allele “C” may be a protective factor of SCZ, while the significance disappeared after correction.

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