RS202059067 NRXN1

Health Risk Chr 2:50346835
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NRXN1
rs267606922 rs1558507406 rs55640811 rs113028018 rs372311299 rs201818223 rs192909520 rs200468214 rs201118246 rs75137449
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