Atrial fibrillation-a complex polygenetic disease.

Eur J Hum Genet · 2021 · PMC8298566 · PMID 33279945

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highly significantno p-value reported

Another highly significant SNP identified through GWAS is rs2106261 ( NC_000016.9 ( NM_001164766.2 :g.73051620C>T)) located on chromosome 16q22 intronic to the transcription factor gene ZFHX3 [ 19 ].

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