RS765086319 FA2H

Health Risk Chr 16:74726273
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Hereditary spastic paraplegia
Hereditary spastic paraplegia 35
Inborn genetic diseases
Hereditary spastic paraplegia
Hereditary spastic paraplegia 35
Other Variants in FA2H
rs1567633766 rs121918217 rs387907039 rs759947457 rs387907040 rs587776891 rs387907172 rs794729214 rs794729215 rs797045569
Ask Dr. Hemsworth about this variant