RS376222680 SYP

Health Risk Chr X:49191511
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SYP
rs2147882650 rs2147884161 rs137852561 rs145093168 rs201427270 rs200470034 rs139475570 rs2065508863 rs1557103139 rs1557103814
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