RS374511482 GNPTG

Health Risk Chr 16:1363025
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in GNPTG
rs193302856 rs193302859 rs137852884 rs137852885 rs193302848 rs193302847 rs193302849 rs193302853 rs193302854 rs193302855
Ask Dr. Hemsworth about this variant