RS2134950483 CTSF

Health Risk Chr 11:66564893
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Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder
Inborn genetic diseases
Neurodevelopmental disorder
Other Variants in CTSF
rs397514731 rs397514732 rs397514733 rs753084727 rs797045136 rs141915593 rs148611356 rs1555058286 rs141345438 rs573483617
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