RS793888521 PCSK9

Health Risk Chr 1:55052364
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hypercholesterolemia
familial
1
autosomal dominant
3
Familial hypercholesterolemia
Hypercholesterolemia
familial
1
autosomal dominant
3
Familial hypercholesterolemia
Other Variants in PCSK9
rs28942111 rs28942112 rs137852912 rs67608943 rs28362286 rs794728683 rs141502002 rs374603772 rs41297883 rs28362270
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