RS730880266 NAGS

Health Risk Chr 17:44006638
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hyperammonemia
type III
Inborn genetic diseases
Hyperammonemia
type III
Inborn genetic diseases
Other Variants in NAGS
rs104894604 rs730880267 rs730880303 rs121912591 rs104894605 rs104894606 rs104894607 rs886042831 rs371886833 rs150004962
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