RS398122407 VPS33B

Health Risk Chr 15:91004872
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What This Variant Does
"CLNSIG=5
Associated Conditions
Arthrogryposis
renal dysfunction
and cholestasis 1
Inborn genetic diseases
VPS33B-related disorder
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Cholestasis
progressive familial intrahepatic
12
Arthrogryposis
renal dysfunction
and cholestasis 1
Inborn genetic diseases
VPS33B-related disorder
Other Variants in VPS33B
rs121434383 rs121434384 rs121434385 rs794726658 rs1555460030 rs398122408 rs864622006 rs145092724 rs886043445 rs201436915
Ask Dr. Hemsworth about this variant