RS11568437 SLC7A7

Health Risk Chr 14:22812923 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Lysinuric protein intolerance
Autoinflammatory syndrome
Inborn genetic diseases
Lysinuric protein intolerance
Autoinflammatory syndrome
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
Other Variants in SLC7A7
rs121908676 rs72552272 rs121908678 rs121908679 rs386833792 rs386833793 rs386833794 rs386833796 rs386833797 rs386833798
Ask Dr. Hemsworth about this variant