RS387906301 LDLR

Health Risk Chr 19:11100292
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What This Variant Does
"aka c.137_142delGCGATG or p.Asp47_Gly48del reported in ClinVar as pathogenic for familial hyperchole...
Associated Conditions
Hypercholesterolemia
familial
1
Hypercholesterolemia
familial
1
Other Variants in LDLR
rs121908024 rs121908025 rs121908026 rs28942082 rs28942083 rs121908028 rs121908029 rs121908030 rs28942078 rs28942079
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