RS139043155 LDLR
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What This Variant Does
"aka c.798T>
Associated Conditions
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
Homozygous familial hypercholesterolemia
Cardiovascular phenotype
See cases
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
Homozygous familial hypercholesterolemia
Cardiovascular phenotype
See cases
Other Variants in LDLR