RS797044450 GH1

Health Risk Chr 17:63918011
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant isolated somatotropin deficiency
Autosomal dominant isolated somatotropin deficiency
Other Variants in GH1
rs1907472729 rs137853219 rs2509253023 rs797044449 rs137853220 rs71640277 rs863223306 rs2144738731 rs137853221 rs863223307
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