RS200649090 INTS1

Health Risk Chr 7:1503021
Upload your DNA to see your genotype for this variant.
Associated Conditions
Neurodevelopmental disorder with cataracts
poor growth
and dysmorphic facies
Inborn genetic diseases
Neurodevelopmental disorder with cataracts
poor growth
and dysmorphic facies
Inborn genetic diseases
Other Variants in INTS1
rs2483311809 rs200828819 rs2128544907 rs138397380 rs2128532901 rs199728337 rs202052814 rs138307850 rs373326766 rs1782841146
Ask Dr. Hemsworth about this variant