RS28940272 VPS13B

Health Risk Chr 8:99820031
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What This Variant Does
"[OMIM:[[Cohen Syndrome]]]
Associated Conditions
Cohen syndrome
Inborn genetic diseases
Malignant tumor of urinary bladder
Cohen syndrome
Inborn genetic diseases
Malignant tumor of urinary bladder
Other Variants in VPS13B
rs180177327 rs120074149 rs120074150 rs120074151 rs120074152 rs120074153 rs120074154 rs180177329 rs386834054 rs386834055
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