RS1060502161 ELAC2

Health Risk Chr 17:13016933
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 17
Inborn genetic diseases
Combined oxidative phosphorylation defect type 17
Inborn genetic diseases
Other Variants in ELAC2
rs387906327 rs119484086 rs397515463 rs397515464 rs397515465 rs397515466 rs201830045 rs149733287 rs9895963 rs1555571246
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