RS140466069 SPTBN4

Health Risk Chr 19:40557321
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SPTBN4
rs1114167445 rs1555815437 rs1555818396 rs777273785 rs1555721549 rs1599794560 rs1599759068 rs1599819198 rs2080330778 rs2080555011
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