RS863224028 GFER

Health Risk Chr 16:1984415
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Mitochondrial disease
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
Mitochondrial disease
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
Other Variants in GFER
rs121908192 rs375792737 rs771809901 rs183638147 rs373135339 rs1555486560 rs1597063051 rs1597063303 rs201762532 rs1028553365
Ask Dr. Hemsworth about this variant