RS1064795772 SLC25A46

Health Risk Chr 5:110739129
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neuropathy
hereditary motor and sensory
type 6B
Pontocerebellar hypoplasia
type 1E
Inborn genetic diseases
Neuropathy
hereditary motor and sensory
type 6B
Pontocerebellar hypoplasia
type 1E
Other Variants in SLC25A46
rs1057519416 rs1057518748 rs1057518749 rs1057518750 rs746681765 rs1057519294 rs1057519295 rs1057519296 rs751900293 rs149585060
Ask Dr. Hemsworth about this variant