RS796065308 PNPLA2

Health Risk Chr 11:822522
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neutral lipid storage myopathy
Inborn genetic diseases
Neutral lipid storage myopathy
Inborn genetic diseases
Other Variants in PNPLA2
rs796065303 rs121918259 rs796065304 rs121918260 rs777539013 rs397514625 rs869320738 rs796065307 rs796065309 rs796065310
Ask Dr. Hemsworth about this variant