RS141222937 GNPTAB

Health Risk Chr 12:101786138
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Associated Conditions
Mucolipidosis type II
Pseudo-Hurler polydystrophy
Inborn genetic diseases
Mucolipidosis type II
Pseudo-Hurler polydystrophy
Inborn genetic diseases
Other Variants in GNPTAB
rs281865025 rs137852895 rs137852896 rs137852897 rs137852898 rs281865038 rs137852899 rs281865031 rs281865029 rs281865027
Ask Dr. Hemsworth about this variant