RS776743373 OCRL

Health Risk Chr X:129562373
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What This Variant Does
"CLNSIG=5
Associated Conditions
Lowe syndrome
Dent disease type 2
Neurodevelopmental delay
Lowe syndrome
Dent disease type 2
Neurodevelopmental delay
Other Variants in OCRL
rs387906484 rs137853260 rs137853261 rs137853262 rs137853263 rs2124412922 rs2124388022 rs137853831 rs137853846 rs137853852
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