RS281860275 CSF1R

Health Risk Chr 5:150056214
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CSF1R
rs281860279 rs281860269 rs281860267 rs281860274 rs387906662 rs281860268 rs281860271 rs281860281 rs281860277 rs397515556
Ask Dr. Hemsworth about this variant