RS1801961640 CSNK2B

Health Risk Chr 6:31668619
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Associated Conditions
Inborn genetic diseases
Poirier-Bienvenu neurodevelopmental syndrome
Medulloblastoma WNT activated
Inborn genetic diseases
Poirier-Bienvenu neurodevelopmental syndrome
Medulloblastoma WNT activated
Other Variants in CSNK2B
rs1085307703 rs1131692161 rs1554169460 rs1554169462 rs1554169990 rs1554169967 rs1554169984 rs1562045237 rs1562050885 rs1583610622
Ask Dr. Hemsworth about this variant