RS552141388 NDUFAF6

Health Risk Chr 8:95025010
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NDUFAF6
rs137853184 rs202047755 rs863223932 rs863223931 rs201732170 rs1554669910 rs201088736 rs768273248 rs1057519084 rs1057519085
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