RS1057519063 VPS33B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Arthrogryposis
renal dysfunction
and cholestasis 1
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Cholestasis
progressive familial intrahepatic
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Arthrogryposis
renal dysfunction
and cholestasis 1
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Cholestasis
progressive familial intrahepatic
Other Variants in VPS33B