RS398124502 PKHD1

Health Risk Chr 6:51747927
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What This Variant Does
"rs398124502, also known as c. 9689del A. or p.Asp3230fs, is a SNP in the PKHD1 gene on chromosome 6....
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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