RS149288103 NCSTN

Health Risk Chr 1:160349008
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NCSTN
rs771414318 rs2525536152 rs2525537394 rs1361408137 rs200634807 rs2101899012 rs374951668 rs2101906549 rs375632985 rs2101909450
Ask Dr. Hemsworth about this variant