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Hypochondroplasia

From SNPedia

At a minimum, these SNPs are known to be related, and others may also be

 Max Magnitude
rs289288680
rs289330680
rs5877787690
rs5877787730
rs5877787750
rs5877787760
rs5877788010
rs5877788110
rs5877788160
rs5877788170

Hypochondroplasia is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 FGFR3 gene, resulting in a disproportionately short stature, micromelia, and a head that appears large when compared with the underdeveloped portions of the body.

Hypochondroplasia is classified as a form short-limbed dwarfism, and although it shows some resemblance to achondroplasia (also associated with FGFR3 mutations), it is usually milder.Wikipedia