Barely Significant
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Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.

Hered Cancer Clin Pract · 2022 · PMC8832647 · PMID 35144679

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp < .0001actually significant
The highly significant difference ( p < .0001) between the proportion of referred members who were documented as racial/ethnic minorities in the EMR (13%) and the proportion in the overall KPNW adult population (19%) strongly suggests disparities in access to referrals between racial and ethnic groups [ 35 ].

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