Case-control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India.

BMC Pediatr · 2023 · PMC10268439 · PMID 37322441

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a weak trendno p-value reported

Variant rs11874 in GOSR2 had nominal association (χ 2 = 3.81; p = 0.051) and rs185531658 an intergenic SNP on Chr 5 [ 39 ] showed association on Fisher’s test as allele counts were low ( p = 0.043) while rs659366 in UCP2 and rs2388896 intergenic SNP demonstrated a weak trend of association (Table 1 ).

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