RS141993646 IFT140

Health Risk Chr 16:1587282
Upload your DNA to see your genotype for this variant.
Associated Conditions
Saldino-Mainzer syndrome
Retinal dystrophy
Inborn genetic diseases
Saldino-Mainzer syndrome
Retinal dystrophy
Inborn genetic diseases
Other Variants in IFT140
rs387907192 rs376586707 rs387907193 rs431905506 rs201188361 rs587776909 rs431905520 rs431905521 rs199826737 rs431905522
Ask Dr. Hemsworth about this variant