RS71640277 GH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant isolated somatotropin deficiency
Short stature due to growth hormone qualitative anomaly
Isolated growth hormone deficiency type IB
Ateleiotic dwarfism
Inborn genetic diseases
Autosomal dominant isolated somatotropin deficiency
Autosomal dominant isolated somatotropin deficiency
Short stature due to growth hormone qualitative anomaly
Isolated growth hormone deficiency type IB
Ateleiotic dwarfism
Inborn genetic diseases
Autosomal dominant isolated somatotropin deficiency
Other Variants in GH1