RS372054380 RTN4IP1

Health Risk Chr 6:106622936
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What This Variant Does
"CLNSIG=5
Associated Conditions
Optic atrophy 10 with or without ataxia
intellectual disability
and seizures
Optic atrophy
Inborn genetic diseases
Optic atrophy 10 with or without ataxia
intellectual disability
and seizures
Optic atrophy
Inborn genetic diseases
Other Variants in RTN4IP1
rs200457692 rs143924605 rs1582392486 rs1776423674 rs771414313 rs145695118 rs751989550 rs749329916 rs1776734650 rs138612238
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