RS34901902 GNPTAB

Health Risk Chr 12:101764860
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mucopolysaccharidosis
MPS-III-A
Mucolipidosis type II
Pseudo-Hurler polydystrophy
Inborn genetic diseases
Mucopolysaccharidosis
MPS-III-A
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