RS143275858 PCSK9

Health Risk Chr 1:55058106
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hypercholesterolemia
familial
1
autosomal dominant
3
Familial hypercholesterolemia
Cardiovascular phenotype
Hypercholesterolemia
familial
1
autosomal dominant
3
Familial hypercholesterolemia
Cardiovascular phenotype
Other Variants in PCSK9
rs28942111 rs28942112 rs137852912 rs67608943 rs28362286 rs793888521 rs794728683 rs141502002 rs374603772 rs41297883
Ask Dr. Hemsworth about this variant