RS119484086 ELAC2

Health Risk Chr 17:12992957
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What This Variant Does
"[OMIM:?]
Associated Conditions
Prostate cancer
hereditary
2
Combined oxidative phosphorylation defect type 17
Inborn genetic diseases
Prostate cancer
hereditary
2
Combined oxidative phosphorylation defect type 17
Inborn genetic diseases
Other Variants in ELAC2
rs387906327 rs397515463 rs397515464 rs397515465 rs397515466 rs201830045 rs149733287 rs9895963 rs1555571246 rs1060502161
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