RS387906886 MAN1B1

Health Risk Chr 9:137101088
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rafiq syndrome
MAN1B1-related disorder
Inborn genetic diseases
See cases
Rafiq syndrome
MAN1B1-related disorder
Inborn genetic diseases
See cases
Other Variants in MAN1B1
rs387906885 rs1564311909 rs181795958 rs374247020 rs794729645 rs797045688 rs186504463 rs114057640 rs145524720 rs138658585
Ask Dr. Hemsworth about this variant