RS199754807 ERCC8;NDUFAF2

Health Risk Chr 5:60945369
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 10
Cockayne syndrome type 1
nuclear type 1
NDUFAF2-related disorder
Mitochondrial complex I deficiency
nuclear type 10
Cockayne syndrome type 1
nuclear type 1
NDUFAF2-related disorder
Other Variants in ERCC8;NDUFAF2
rs121434324 rs772489808
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