RS119490108 GRHPR

Health Risk Chr 9:37426545
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Primary hyperoxaluria
type II
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Primary hyperoxaluria
type II
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Other Variants in GRHPR
rs80356708 rs180177321 rs672601351 rs180177322 rs180177307 rs796052077 rs180177311 rs180177320 rs180177319 rs180177304
Ask Dr. Hemsworth about this variant