RS61752971 OCRL

Health Risk Chr X:129557953
Upload your DNA to see your genotype for this variant.
Associated Conditions
Developmental cataract
Lowe syndrome
Dent disease type 2
Nephrolithiasis/nephrocalcinosis
Genetic developmental and epileptic encephalopathy
Epilepsy
Developmental cataract
Lowe syndrome
Dent disease type 2
Nephrolithiasis/nephrocalcinosis
Genetic developmental and epileptic encephalopathy
Epilepsy
Other Variants in OCRL
rs387906484 rs137853260 rs137853261 rs137853262 rs137853263 rs2124412922 rs2124388022 rs137853831 rs137853846 rs137853852
Ask Dr. Hemsworth about this variant