RS149614625 IFT172
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Short-rib thoracic dysplasia 10 with or without polydactyly
Retinitis pigmentosa 71
Retinitis pigmentosa
Bardet-Biedl syndrome 20
IFT172-related disorder
Short-rib thoracic dysplasia 10 with or without polydactyly
Retinitis pigmentosa 71
Retinitis pigmentosa
Bardet-Biedl syndrome 20
IFT172-related disorder
Other Variants in IFT172