RS766081510 SLX4

Health Risk Chr 16:3590268
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Associated Conditions
Fanconi anemia
Inborn genetic diseases
Fanconi anemia complementation group P
Fanconi anemia
Inborn genetic diseases
Fanconi anemia complementation group P
Other Variants in SLX4
rs1596534281 rs1218169126 rs773642409 rs1567178071 rs201582780 rs146054214 rs144326379 rs111738042 rs142205392 rs878855162
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