RS387906885 MAN1B1

Health Risk Chr 9:137101607
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rafiq syndrome
Inborn genetic diseases
Rafiq syndrome
Inborn genetic diseases
Other Variants in MAN1B1
rs1564311909 rs387906886 rs181795958 rs374247020 rs794729645 rs797045688 rs186504463 rs114057640 rs145524720 rs138658585
Ask Dr. Hemsworth about this variant