RS387906307 LDLR

Health Risk Chr 19:11089411
Upload your DNA to see your genotype for this variant.
What This Variant Does
"aka c.-138delT reported in ClinVar as pathogenic for familial hypercholesterolemia and therefore inc...
Associated Conditions
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
Cardiovascular phenotype
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
Cardiovascular phenotype
Other Variants in LDLR
rs121908024 rs121908025 rs121908026 rs28942082 rs28942083 rs121908028 rs121908029 rs121908030 rs28942078 rs28942079
Ask Dr. Hemsworth about this variant