RS769333468 VPS33B

Health Risk Chr 15:91009799
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Arthrogryposis
renal dysfunction
and cholestasis 1
Cholestasis
progressive familial intrahepatic
12
Keratoderma-ichthyosis-deafness syndrome
autosomal recessive
Arthrogryposis
renal dysfunction
and cholestasis 1
Cholestasis
progressive familial intrahepatic
12
Keratoderma-ichthyosis-deafness syndrome
Other Variants in VPS33B
rs121434383 rs121434384 rs121434385 rs794726658 rs1555460030 rs398122407 rs398122408 rs864622006 rs145092724 rs886043445
Ask Dr. Hemsworth about this variant