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. 2020 Nov 20;38(2):365–374. doi: 10.1007/s10815-020-02006-y

Table 2.

HBB mutation and SNPs genotyping results for case 2.

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Legend: Genotype of parents and embryos assessing a CD17 mutation and CD26 mutation of the HBB gene plus 19 SNPs closely associated with the mutation. P = paternal, M = maternal, 1 = allele 1, 2 = allele 2, red block = mutation, pink/purple/Gy = no mutation. Parental haplotypes represented by “P1/P2” meaning paternal haplotype 1 and paternal haplotype 2; same for maternal haplotypes are labeled and color coded for ease of interpretation