Article

<i>ADRA2A</i>and<i>IRX1</i>are putative risk genes for Raynaud’s phenomenon

2022-10-21

Abstract excerpt

Raynaud’s phenomenon (RP) is a common vasospastic disorder that causes severe pain and ulcers, but despite its high reported heritability, no causal genes have been robustly identified. We conducted a genome-wide association study including 5,147 RP cases and 439,294 controls, based on diagnoses from electronic health records, and identified three unreported genomic regions associated with the risk of RP ( p< 5×10...

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Literature Corpus work: 8528d9e6-202a-5626-bfa7-43ffed730cf0
DOI: 10.1101/2022.10.19.22281276

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