RS754097561 MCOLN1

Health Risk Chr 19:7529689
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Mucolipidosis type IV
Inborn genetic diseases
Lisch epithelial corneal dystrophy
Mucolipidosis type IV
Mucolipidosis type IV
Inborn genetic diseases
Lisch epithelial corneal dystrophy
Mucolipidosis type IV
Other Variants in MCOLN1
rs104886461 rs121908371 rs121908372 rs121908373 rs121908374 rs797044824 rs767122713 rs755042147 rs797044822 rs797044817
Ask Dr. Hemsworth about this variant