RS776173779 TNFRSF11A

Health Risk Chr 18:62369257
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in TNFRSF11A
rs879253796 rs796051862 rs121908655 rs121908656 rs121908658 rs121908659 rs772863037 rs771249524 rs886037749 rs1555767678
Ask Dr. Hemsworth about this variant