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Fig. 3 | Genome Medicine

Fig. 3

From: NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Fig. 3

Variant interpretation using the NARD. a MAF differences of SNPs shared between the NARD and gnomAD. The y-axis denotes the MAF of SNPs in worldwide populations (ALL) or EAS from the gnomAD. Color represents the MAF of SNPs in 1779 Northeast Asians from the NARD. b Number of uncommon (MAF < 5%) protein-altering variants (missense, nonsense, frameshift, and splicing variants) after filtration using the gnomAD with/without NARD. Variant catalogue from the gnomAD (exome) was applied. ***P < 0.0001 by two-tailed Mann-Whitney U test (compared with gnomAD-EAS + NARD)

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Genome Medicine

ISSN: 1756-994X

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