RS1662848905 MYCN

Health Risk Chr 2:15945735
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Associated Conditions
Inborn genetic diseases
Feingold syndrome type 1
Inborn genetic diseases
Feingold syndrome type 1
Other Variants in MYCN
rs104893646 rs104893647 rs104893648 rs121913667 rs113994115 rs1558534266 rs886039427 rs886039428 rs886041290 rs886041801
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