RS186859701 NPRL3

Health Risk Chr 16:110557
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Associated Conditions
Epilepsy
familial focal
with variable foci 3
Inborn genetic diseases
Epilepsy
familial focal
with variable foci 3
Inborn genetic diseases
Other Variants in NPRL3
rs886037958 rs886037959 rs886037960 rs886037961 rs886037962 rs1064795838 rs746082270 rs547498080 rs367664536 rs1555444207
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