RS755131489 SCYL1

Health Risk Chr 11:65526147
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SCYL1
rs141670485 rs143168314 rs201043872 rs201581270 rs1855366408 rs773812714 rs1320473430 rs2496024369 rs2495967037 rs1481969607
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