RS750413238 CSF1R

Health Risk Chr 5:150078194
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Associated Conditions
Parkinsonian disorder
Inborn genetic diseases
Parkinsonian disorder
Inborn genetic diseases
Other Variants in CSF1R
rs281860279 rs281860269 rs281860267 rs281860274 rs387906662 rs281860268 rs281860271 rs281860281 rs281860277 rs397515556
Ask Dr. Hemsworth about this variant