FANCG and Friedreich ataxia: We identified 57 different, rare heterozygous, germline FANCG variants (Figure 1A; Table 1) including 13 frameshift, stop‐gain, or spliceogenic variants considered as GPVs (localized before the most N‐terminal GPV identified in FA‐G patients, c.1795_1804del—ClinVar ID: 6718).