RS180177239 AGXT

Health Risk Chr 2:240873022
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What This Variant Does
"CLNSIG=255
Associated Conditions
Primary hyperoxaluria
type I
Severe combined immunodeficiency
autosomal recessive
T cell-negative
B cell-negative
NK cell-negative
due to adenosine deaminase deficiency
Primary hyperoxaluria
Primary hyperoxaluria
type I
Severe combined immunodeficiency
autosomal recessive
T cell-negative
B cell-negative
Other Variants in AGXT
rs121908520 rs121908521 rs121908522 rs121908523 rs121908524 rs121908525 rs121908526 rs121908527 rs121908528 rs121908530
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