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Table 5 Genotype distribution of MTHFR in DSM and neonatal jaundice in the DS child

From: MTHFR gene polymorphism and associated nutritional deficiency in the etiology and pathogenesis of Down syndrome

Genotype

DSM group

No neonatal jaundice

n, f(%)

Neonatal jaundice

n, f(%)

OR (CI)

p value

CC

31 (26.2)

11 (9.3)

Reference

Reference

CT

45 (38.1)

31 (26.2)

1.9 (0.8 to 4.4)

p = 0.1128NS

  1. n number of genotype, f frequency, OR odds ratio, CI 95% confidence interval, NS not significant