RS398124484 PKHD1

Health Risk Chr 6:52026048
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What This Variant Does
"rs398124484, also known as c.3761_3762del insG or p.Ala1254fs, is a SNP in the PKHD1 gene on chromos...
Associated Conditions
Autosomal recessive polycystic kidney disease
Polycystic kidney disease 4
PKHD1-related disorder
Autosomal recessive polycystic kidney disease
Polycystic kidney disease 4
PKHD1-related disorder
Other Variants in PKHD1
rs137852944 rs28937907 rs137852946 rs137852947 rs137852948 rs137852949 rs137852950 rs398124475 rs398124476 rs398124477
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