RS886041801 MYCN

Health Risk Chr 2:15942504
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in MYCN
rs104893646 rs104893647 rs104893648 rs121913667 rs113994115 rs1558534266 rs886039427 rs886039428 rs886041290 rs886042150
Ask Dr. Hemsworth about this variant