Single-cell polygenic risk scores dissect cellular and molecular heterogeneity of complex human diseases.

5h ) contained a nominally significant GWAS 30 variant rs886125 (GWAS P = 0.019, β = −0.149, effect/alternative allele = G) and was coaccessible (coaccessibility = 0.367) with MYL2 , a widely recognized HCM gene 80 .

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