RS104893647 MYCN

Health Risk Chr 2:15945879
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What This Variant Does
"[OMIM:?]
Associated Conditions
Feingold syndrome type 1
Inborn genetic diseases
Feingold syndrome type 1
Inborn genetic diseases
Other Variants in MYCN
rs104893646 rs104893648 rs121913667 rs113994115 rs1558534266 rs886039427 rs886039428 rs886041290 rs886041801 rs886042150
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