Article

Characterization of variants associated with Cerebral Small Vessel Disease identifies a functional SNV in Versican

2026-03-17

Abstract excerpt

<h4>Background</h4> Single nucleotide variants in the non-coding genome can significantly alter disease risk, but identifying the function of SNVs is a challenge. Increasing numbers of variants of unknown significance have been associated with the risk of Stroke, Cerebral Small Vessel Disease and burden of White Matter Hyperintensities, but without biological validation, the significance of these findings is unce...

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Literature Corpus work: 4573993a-1fab-51a8-9e74-5ba175b51a96
DOI: 10.64898/2026.03.16.712010

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