RS2078522740 KDM6B

Health Risk Chr 17:7845871
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Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
Inborn genetic diseases
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
Other Variants in KDM6B
rs148641957 rs199964822 rs1419917079 rs769566928 rs957520585 rs2078587931 rs59062945 rs748243814 rs2151375529 rs2078638223
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