RS2052290589 CTCF

Health Risk Chr 16:67626598
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CTCF
rs879255570 rs879255571 rs879255516 rs148681672 rs886039600 rs886041997 rs886041901 rs1064796062 rs1131691283 rs1555535156
Ask Dr. Hemsworth about this variant