RS104894705 NDUFS7

Health Risk Chr 19:1391005 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 3
Leigh syndrome
Mitochondrial complex I deficiency
nuclear type 3
Leigh syndrome
Population Frequencies
gnomAD ALL
0%
Other Variants in NDUFS7
rs121434479 rs1568985256 rs140236960 rs863224113 rs11551664 rs370241999 rs573586959 rs375120743 rs144570086 rs201222388
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