Fig. 2: ARHGAP29 protein domains with variants: our findings above the figure; reported ones below the figure; dashed line, rare variants discovered through direct sequencing on candidate regions from GWAS studies; continuous lines, rare variants found by exome sequencing. | European Journal of Human Genetics

Fig. 2: ARHGAP29 protein domains with variants: our findings above the figure; reported ones below the figure; dashed line, rare variants discovered through direct sequencing on candidate regions from GWAS studies; continuous lines, rare variants found by exome sequencing.

From: Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC)

Fig. 2

Symbols for ACMG classification of variants in Varsome: Δ, likely benign; #, VUS, and underlined variants, pathogenic/likely pathogenic.

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