RS770116680 P4HTM

Health Risk Chr 3:49005084
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in P4HTM
rs182812551 rs1576610000 rs757914897 rs1339145374 rs1413442651 rs2471528764 rs1361197028 rs760453324 rs2471545464 rs758831068
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