RS398122392 CRYGC

Health Risk Chr 2:208128258
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cataract 2
multiple types
Inborn genetic diseases
Cataract 2
multiple types
Inborn genetic diseases
Other Variants in CRYGC
rs200505176 rs2468835222 rs777748323 rs144295934 rs2468835044 rs2105857780 rs2105857887 rs2105857937 rs2105857860 rs141474796
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