RS121908576 BCS1L

Health Risk Chr 2:218661153
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial complex III deficiency nuclear type 1
BCS1L-related disorder
GRACILE syndrome
Pili torti-deafness syndrome
Leigh syndrome
Autosomal recessive BCS1L-related disorders
Mitochondrial complex III deficiency nuclear type 1
BCS1L-related disorder
GRACILE syndrome
Pili torti-deafness syndrome
Leigh syndrome
Autosomal recessive BCS1L-related disorders
Other Variants in BCS1L
rs121908571 rs121908572 rs121908573 rs121908574 rs28937590 rs121908575 rs121908577 rs121908578 rs121908579 rs121908580
Ask Dr. Hemsworth about this variant