RS886039839 PCSK9

Health Risk Chr 1:55040022
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypercholesterolemia
familial
1
Cardiovascular phenotype
autosomal dominant
3
Hypercholesterolemia
familial
1
Cardiovascular phenotype
autosomal dominant
3
Other Variants in PCSK9
rs28942111 rs28942112 rs137852912 rs67608943 rs28362286 rs793888521 rs794728683 rs141502002 rs374603772 rs41297883
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