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Secondary findings in a large Pakistani cohort tested with whole genome sequencing.


ABSTRACT: Studies on genomic secondary findings (SFs) are diverse in participants' characteristics, sequencing methods, and versions of the ACMG SF list. Based on whole genome sequencing and the version 3.1 of the ACMG SF list, we studied SFs in 863 individuals from five different regions in Pakistan. We identified 24 ACMG SFs in 23 (2.7%) of 863 individuals: 18 of 24 were related to cardiovascular disease and four to cancer syndromes. In addition to ACMG SFs, we identified 16 (1.9%) participants with pathogenic and likely pathogenic variants in genes that were not related to the participants' clinical conditions but with clear medical actionability (non-ACMG SFs): 4 of 16 were related to eye diseases, two to metabolic disorders, and two to urinary system disorders. By testing a large Pakistani cohort with whole genome sequencing, we concluded that in countries such as Pakistan, the ACMG SF list could be expanded, and our non-ACMG SF list is one example.

SUBMITTER: Skrahin A 

PROVIDER: S-EPMC9838216 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature

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Secondary findings in a large Pakistani cohort tested with whole genome sequencing.

Skrahin Aliaksandr A   Cheema Huma Arshad HA   Hussain Maqbool M   Rana Nuzhat Noureen NN   Rehman Khalil Ur KU   Kumar Raman R   Oprea Gabriela G   Ameziane Najim N   Rolfs Arndt A   Skrahina Volha V  

Life science alliance 20230112 3


Studies on genomic secondary findings (SFs) are diverse in participants' characteristics, sequencing methods, and versions of the ACMG SF list. Based on whole genome sequencing and the version 3.1 of the ACMG SF list, we studied SFs in 863 individuals from five different regions in Pakistan. We identified 24 ACMG SFs in 23 (2.7%) of 863 individuals: 18 of 24 were related to cardiovascular disease and four to cancer syndromes. In addition to ACMG SFs, we identified 16 (1.9%) participants with pat  ...[more]

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