RS794728683 PCSK9

Health Risk Chr 1:55052398
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypercholesterolemia
autosomal dominant
3
familial
1
Familial hypercholesterolemia
Homozygous familial hypercholesterolemia
Cardiovascular phenotype
Hypercholesterolemia
autosomal dominant
3
familial
1
Familial hypercholesterolemia
Homozygous familial hypercholesterolemia
Other Variants in PCSK9
rs28942111 rs28942112 rs137852912 rs67608943 rs28362286 rs793888521 rs141502002 rs374603772 rs41297883 rs28362270
Ask Dr. Hemsworth about this variant