RS201003932 LBR
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Associated Conditions
Greenberg dysplasia
Inborn genetic diseases
Reynolds syndrome
Regressive spondylometaphyseal dysplasia
Pelger-Huët anomaly
Greenberg dysplasia
Inborn genetic diseases
Reynolds syndrome
Regressive spondylometaphyseal dysplasia
Pelger-Huët anomaly
Other Variants in LBR