RS180177201 AGXT

Health Risk Chr 2:240868891
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary hyperoxaluria
type I
Nephrotic syndrome
AGXT-related disorder
Alanine glyoxylate aminotransferase deficiency
Inborn genetic diseases
Primary hyperoxaluria
type I
AGXT-related disorder
Primary hyperoxaluria
type I
Primary hyperoxaluria
type I
Nephrotic syndrome
AGXT-related disorder
Other Variants in AGXT
rs121908520 rs121908521 rs121908522 rs121908523 rs121908524 rs121908525 rs121908526 rs121908527 rs121908528 rs121908530
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