RS369726600 VPS33B

Health Risk Chr 15:91009801
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Associated Conditions
Inborn genetic diseases
Cholestasis
progressive familial intrahepatic
12
Arthrogryposis
renal dysfunction
and cholestasis 1
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Inborn genetic diseases
Cholestasis
progressive familial intrahepatic
12
Arthrogryposis
renal dysfunction
Other Variants in VPS33B
rs121434383 rs121434384 rs121434385 rs794726658 rs1555460030 rs398122407 rs398122408 rs864622006 rs145092724 rs886043445
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