RS778958318 CPS1

Health Risk Chr 2:210573338
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital hyperammonemia
type I
Inborn genetic diseases
Congenital hyperammonemia
type I
Inborn genetic diseases
Other Variants in CPS1
rs753751183 rs121912592 rs121912593 rs28940283 rs121912595 rs121912596 rs1559129372 rs587780323 rs727502824 rs150966847
Ask Dr. Hemsworth about this variant