RS869312922 RFXANK

Health Risk Chr 19:19197622
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
MHC class II deficiency
Inborn genetic diseases
MHC class II deficiency
Other Variants in RFXANK
rs759667201 rs104894709 rs201778172 rs754519730 rs115220304 rs114064359 rs1568578781 rs778357787 rs1599784374 rs749579925
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